Vagas PCD na IQVIA

    57 vagas abertas, atualizado em 23/09/2026

    A IQVIA tem 57 vagas para pessoas com deficiência em São Paulo - SP, principalmente nas áreas de Saúde, Atendimento e Administrativo. As vagas são publicadas pela empresa no PCD Online, onde fica a candidatura oficial. Este portal não é o site oficial da IQVIA.

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    Vaga PCD Clinical Scientist in CNS - LATAM (Pessoa Com Deficiência - PCD)

    IQVIA
    São Paulo - SP

    Somente PCD - IQVIA provides scientific services spanning clinical trials, real world evidence, and consulting in all areas of the product lifecycle. The Patient Centered Solutions (PCS) team leads the industry in generating data to ensure that the patient voice is incorporated into the development and commercialization of medication and other drug/non-drug interventions. We focus on understanding and meeting the needs of our clients – mostly life science/pharmaceutical companies – through the application of broad consulting expertise and technical scientific knowledge to design scientifically rigorous research. This research is broad and includes qualitative (e.g. interviews, focus groups), quantitative (e.g. clinical outcome assessments (COAs)/patient-reported outcomes (PROS), preference research) and passive (e.g. digital health technology tools) approaches to understand patient, caregiver and healthcare professional experiences and expectations of disease and treatment. To meet our client expectations and retain the excellent reputation built up over time the IQVIA PCS team is committed to recruiting, training and supporting driven individuals who have both consulting skills and life science skills that can be applied to PCS research activities. Individuals joining us are assured of a rewarding and progressive career in patient-focused research. You’ll have the opportunity to address challenging client issues, across multiple geographies with a hands-on influence in developing and delivering solutions. We operate in a truly multi-cultural, collegial and collaborative work environment that is rich in development and growth. Role & Responsibilities The role-holder will need to be a committed individual, who combines high emotional intelligence and excellent communication skills. They will thrive in a fast-paced environment and be comfortable managing conflicting priorities. The environment is dynamic and ever-changing, moving at the pace of our clients’ needs and the candidate will be expected to understand the sense of urgency that is synonymous with the business. As a Consultant, ClinRO Services within the PCS team at IQVIA, you will directly administer assessments to participants in a clinical trial, or evaluate the quality of assessments performed by others and provide feedback regarding interview technique and scoring. Responsibilities include: Review of scales administered by raters in a clinical trial to ensure that assessments are being conducted in a standardized manner to ensure data reliability.Evaluation the quality of assessments, conducting live interactions with raters to discuss assessment methodology, scoring technique, and to provide guidance, as necessary.Evaluate case data and appropriately prepare for discussions with raters (e.g., prepared to discuss relevant issues and scale items, and have necessary documents available).Complete rater interactions and assigned tasks as scheduled.Responsible for timely submission of all documentation associated with assigned tasks.Participate in all orientation, training and calibration activities as required.Functional assessments of rater performance (e.g., mock interview) and assistance in preparing and disseminating communications.Contacting clinical trial participants remotely (e.g., via proprietary app, Engage) to administer assessments, and will appropriately document resultant information (e.g., notes, scores) What do you need to apply? Minimum of a Master’s degree (MA/MS) in Psychology, Counseling, Psychiatric, Nursing or Social Work, or equivalent.Minimum of 3 years’ clinical experience working with schizophrenia and major depressive disorder populations.Minimum of 3 years clinical experience working administering psychiatric assessments including the PANSS, to these populations is also required.Clinical Trials experience preferred.Advanced level of English. Home based position in Latin America. #LI-Remote #LI-NITINMAHAJAN IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

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    Vaga PCD Pharmacovigilance Specialist (Fluent in English + Italian) (Pessoa Com Deficiência - PCD)

    IQVIA
    São Paulo - SP

    Somente PCD - Job Overview Review, assess, and process safety data and information across service lines, received from various sources. Distribute reports/data to both internal and external third parties following applicable regulations, Standard Operating Procedures (SOPs), and internal guidelines under the guidance and support of senior operation team members. This is a trilingual role requiring fluency in English, Spanish, and Italian. Main Responsibilities Process safety data according to applicable regulations, guidelines, SOPs, and project requirements.Perform pharmacovigilance activities, including collecting and tracking incoming Adverse Events (AEs) and endpoint information, determining initial/update status of incoming events, database entry, coding AEs and products, writing narratives, and literature-related activities.Ensure compliance with quality, productivity, and delivery standards per project requirements.Liaise with different functional team members and healthcare professionals to address project-related issues. Qualifications Bachelor’s degree in Life sciences or a related field (mandatory)Fluency in English and Italian (mandatory) (will be evaluated)Up to 3 years of previous clinical experience (desirable)1 year of pharmacovigilance experience will be highly valued (desirable) What we offer to you: OSDE 310Annual bonus by performanceSalary adjustments during the year according to inflation rates.21 vacations daysWork flexibility100% remote role! IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

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    Vaga PCD RFI Developer 2 (Pessoa Com Deficiência - PCD)

    IQVIA
    São Paulo - SP

    Somente PCD - Job Profile Summary Prepare comprehensive, timely and accurate responses to stakeholders' requests for information to support global sales teams and other internal customers. Essential Functions Research, organize and write corporate capabilities and experience documents for proposals, sales initiatives and customer questionnaires Coordinate the inputs of multiple sources and prepare formal replies to customers' global outsourcing and preferred provider request for information (RFIs) Serve as the principal responder to internal and external requests for information Contribute to improvement initiatives for RFI information storage and retrieval systems Maintain currency in applicable company management and research databases Perform company, industry, and competitor research as required Participate in the development and maintenance of department information sources, templates, and related materials Perform other duties as assigned Education, Experience, Skills and/or Abilities Bachelor's Degree Degree in Life Science, Business Management, Finance, IT or related field At least 3 year work experience in Proposal and/or Contract Management, Marketing, Finance, IT, Business Management / Development or an equivalent combination of education, training and experience Project Demonstrated project management skills Demonstrated problem solving skills Demonstrated verbal and written communication skills Fluency in English written and verbal communication skills (this role is part of a Global team) Ability to build strong customer relationship Knowledge of Microsoft Excel, PowerPoint and Word Knowledge of CRO, Pharmaceutical or related industry will be a plus *Resume/CV must be submitted in English* IQVIA is committed to embracing a diverse and inclusive work environment. Our goal is to attract and retain the best people, regardless of their gender, race, marital status, ethnic origin, national origin, age, disability, sexual orientation, gender identity or any other characteristic. Join us! ⚠️ IQVIA contacts candidates exclusively through its official recruitment channels, including corporate email addresses ending in @iqvia.com and company-authorized recruitment platforms. If you receive a suspicious communication claiming to be from IQVIA through unofficial channels, we recommend that you do not share any personal information and contact us through our official channels for verification. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

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    Vaga PCD Regional Specialist in Argentina or Brazil (Pessoa Com Deficiência - PCD)

    IQVIA
    São Paulo - SP

    Somente PCD - Job OverviewRemote Research Clinical Regional Specialists (RS) are an integral part of remote visit delivery, liaising with clinical teams, clinicians, and investigator sites for remote visits. The RS works in partnership with the RRC Lead providing support with remote visit activities to mitigate risk, control cost, manage project schedule, and ensure customer satisfaction related to assigned project/s. Essential FunctionsSite and Nurse Onboarding- Conduct outreach and training for investigator sites opting into RRC services.- Train and onboard research clinicians, ensuring they are prepared and study-ready.- Manage access to systems like Study Hub and Thinking Cap for both site staff and clinicians. Remote Visit Coordination- Receive and process Visit Request Forms (VRFs).- Assign and confirm clinicians for remote visits.- Coordinate visit logistics including supplies, equipment, and courier services.- Ensure all required documentation (e.g., DOA logs, nurse credentials) is complete and uploaded. Document and Data Management- Maintain and update Smartsheet trackers for sites, visits, and nurses.- Perform quality checks on source documents and ensure timely corrections.- Review uploaded documents in Study Hub and notify relevant stakeholders. Training and Compliance- Deliver study-specific training to sites and clinicians.- Ensure compliance with GCP, ICH, HIPAA, and IQVIA SOPs. Communication and Support- Serve as the primary liaison between sites, nurses, and internal study teams.- Provide ongoing support and retraining to nurses as needed.- Escalate issues to RNPS Lead and ensure resolution. Courier and Logistics Management- Book and track courier shipments for study drug, samples, and documents.- Manage inventory and supply needs for nurses and depots. Requirements • Bachelor's Degree Life sciences or other related field• Typically requires around 2 years of prior relevant experience on site management (Site Coordinator experience or CRA experience) - with visit coordinator skills or relevant project management experience • Advanced level of English is a must. All interviews will be in English. #LI-NRJ #LI-Remote Please, make sure to submit your CV in English. It will be assessed by a global team. ⚠️ IQVIA contacts candidates exclusively through its official recruitment channels, including corporate email addresses ending in @iqvia.com and company-authorized recruitment platforms. If you receive a suspicious communication claiming to be from IQVIA through unofficial channels, we recommend that you do not share any personal information and contact us through our official channels for verification. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

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    Vaga PCD (Senior) Data Team Lead (Pessoa Com Deficiência - PCD)

    IQVIA
    São Paulo - SP

    Somente PCD - Job Overview Independently manage end-to-end delivery of data management services for single/multi-service projects, ensuring quality deliverables on time and within budget, to customer satisfaction. Provide comprehensive data management expertise to Clinical Data Management (CDM) team to provide high quality data management products that meet customer needs. Provide leadership and vision to the team in the areas of project planning, execution, and close-out; financial management; communications; and milestone deliverables. May perform role of Data Team Lead (DTL), Program Lead, Customer Site Manager, and/or a leadership role in a specific CDM task (e.g., Subject Matter Expert (SME). Comply with Good Clinical Practices (GCPs), applicable regulatory guidelines, SOPs, policies, and, where available, CDM guidance documents. Essential Functions Client Management: Serve as primary point of contact for customer on data management deliverables.Manage multiple large studies or program of studies (possibly global) Provide leadership and senior support to DTLs on multiple large global studies/programs of global studies Provide leadership and senior support to DTLs on multiple large global studies/programs of global studies.Provide project management expertise working with customer data managers, key decision makers, and internal team members to manage continuous process improvements, issue escalation, workload projections, and provide technical expertise.Lead direct negotiations with customer, e.g., timelines, financial, process, resources.Maintain strong customer relationships.Ensure open communications with customer and IQVIA management to independently manage and meet contractual obligations.Service Management: Meet with Data Operations Coordinator (DOC) and/or Data Operations team members on a regular basis to ensure milestones meet timelines and quality deliverables.Provide training and development on data management expertise to junior team members.Establish strong communications with Data Operations team, functional leads, project managers and all other stake holders.Independently manage DM service delivery with comprehensive DM process and technical expertise in executing projectsServe as the escalation point for unresolved data issues.Independently work with client data managers, vendors, internal team members for resolutionEnsure appropriate resources are assigned to meet project deliverables.Create and/or review and sign-off on all data management plan (DMP) documents.Ensure service and quality meet agreed upon specifications per the DMP and contract/SOW.Implement proactive quality management plans across multiple projects/programs/customer account. Manage service performance and provide leadership to identify root causes of issues and implement remedial actions.Continuously look for opportunities to improve service.Develop and work with team to implement plan to re-organize and drive change (possibly across a customer account)Ensure timely follow-up and resolution of compliance issues.Serve as Subject Matter Expert (SME)Provide leadership and expertise in a specific CDM task or technology.Serve as customer site lead for one or more customers.Train and mentor junior DTL staff in DM expertiseMay coordinate the work of more junior DTL staff.Independently maintain internal tracking databases and systems Financial Management/Business Development Support: Independently manage SOW/budgetReview financial reports monthly and participate in project reviews as requested.Identify out of scope tasks and track change orders to completion.Participate in pricing discussions across customer account.Serve as Project Manager for single service DM projects, including financial tracking, revenue recognition, and invoicing.Independently support RFP process (review RFP documents, pricing, attend bid defense)Other: Independently bring process improvements and solutions to the CDM team/CDM departmentLead a focus team or global or local best practice team.Communicate lessons learned and/or present in CDM workshop(s)Manage the development and implementation of new technology or tool.Present at professional conferences and/or publish articles in professional journals.Provide review and expert opinion in developing, revising, and maintaining core operating procedures and work instructions.Perform other duties as directed by the functional manager. Qualifications Please note that requirements for this position do not align with an Analyst, Architect Data Entry, Design, Engineering, IT, or Research role. Applicants that do not meet the requirements for the position will not be considered. Bachelor's Degree Health, clinical, biological, or mathematical sciences, or related field Req7 years direct Data Management experience, including 5 or more years as a CDM project lead. Equivalent combination of education, training, and experience.Previous experience and proven competence in managing delivery of multiple global trial

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    Vaga PCD Sr. Contract Negotiation Specialist (North America team) (Pessoa Com Deficiência - PCD)

    IQVIA
    São Paulo - SP

    Somente PCD - Job OverviewUnder general supervision, perform tasks at a country level associated with site activation activities in accordance with applicable local and/or international regulations, standard operating procedures (SOPs), project requirements and contractual/budgetary guidelines. The Contract Specialist is responsible for independently managing the preparation, review, and negotiation of clinical site agreements in support of study start-up activities. This role contributes directly to achieving study timelines by ensuring efficient contract execution while maintaining compliance with applicable regulations, sponsor requirements, and internal policies. Essential Functions Independently draft, review, and negotiate standard clinical trial agreements (e.g., CTAs, CDAs, amendments) with investigative sites and institutions. Manage assigned contract portfolio to support site activation deliverables and study timelines. Act as a primary point of contact for sites and internal teams for contract-related matters, ensuring clear and timely communication. Apply approved negotiation parameters and escalate non-standard terms or higher-risk issues to senior team members or Legal as needed. Collaborate with cross-functional stakeholders (e.g., Site Activation, Clinical Operations, Finance) to align contract terms, including budget-related provisions. Track contract progress and maintain accurate, up-to-date documentation in relevant systems and tools. Identify and proactively address contract-related delays, working to resolve issues and minimize impact on study timelines. Ensure all contracts comply with applicable regulatory requirements, sponsor guidelines, and company policies. Support audit and inspection readiness by maintaining complete and accurate contract files. Contribute to continuous process improvements aimed at enhancing contract cycle times and quality. Manage multiple priorities simultaneously while meeting established timelines and quality expectations. Provide regular status updates and metrics to stakeholders and project teams. Qualifications • Based in Brazil or Argentina. • Bachelor's degree.• 2 to 4 years of experience in clinical research (CRO or pharma) supporting the contract and budget negotiation with sites: direct contract/BGT negotiation experience. • Advanced level of English skills, you will be working in a team that will support sites in North America. Home based role! Please, make sure to submit your CV in English. It will be assessed by a global team. ⚠️ IQVIA contacts candidates exclusively through its official recruitment channels, including corporate email addresses ending in @iqvia.com and company-authorized recruitment platforms. If you receive a suspicious communication claiming to be from IQVIA through unofficial channels, we recommend that you do not share any personal information and contact us through our official channels for verification. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

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    Vaga PCD Gestor de Operações de Navegação do Paciente (Pessoa Com Deficiência - PCD)

    IQVIA
    São Paulo - SP

    Somente PCD - Missão do Cargo Liderar a operação de acompanhamento de pacientes, garantindo qualidade, eficiência, conformidade e alcance dos indicadores da área, além do desenvolvimento e engajamento da equipe. Principais Responsabilidades Gerenciar e desenvolver a equipe de Navegadores de Pacientes.Garantir a execução dos fluxos, processos e protocolos operacionais.Monitorar indicadores de desempenho, qualidade e produtividade, implementando planos de ação quando necessário.Atuar como ponto de escalonamento para situações críticas e desvios operacionais.Assegurar a qualidade dos registros e a integridade das informações nos sistemas.Promover a integração e comunicação entre pacientes, equipes assistenciais, instituições e prestadores.Conduzir treinamentos, calibrações e ações de desenvolvimento da equipe.Liderar iniciativas de melhoria contínua e otimização de processos.Elaborar relatórios gerenciais e acompanhar resultados da operação.Garantir conformidade com políticas de qualidade, privacidade e segurança da informação.Formação e Experiência Requisitos Ensino superior completo, preferencialmente na área da saúde.Experiência em liderança de equipes.Experiência em operações de atendimento, navegação ou acompanhamento de pacientes.Conhecimento do sistema de saúde público e privado.Conhecimento sobre doenças raras e suas jornadas de cuidado.Experiência com gestão de indicadores e melhoria de processos.Conhecimento do Pacote Microsoft Office.Disponibilidade para viagens frequentes.CNH categoria B válidaVeículo próprio em boas condiçõesSeguro vigente.Importante: Esta posição envolve atividades externas que requerem deslocamentos frequentes para atendimento a clientes e visitas técnicas. Por isso, é indispensável que o(a) candidato(a) possua veículo próprio, Carteira Nacional de Habilitação (CNH) válida e documentação do veículo regularizada. Na etapa final do processo seletivo, será realizada a validação documental, com a solicitação do envio das seguintes cópias: CNH (Carteira Nacional de Habilitação);CRLV (Certificado de Registro e Licenciamento do Veículo);Comprovante de seguro. A participação nesta etapa é obrigatória para a continuidade no processo. Diferenciais Pós-graduação em Gestão, Saúde, Projetos ou áreas correlatas.Experiência em programas de suporte ou navegação de pacientes.Vivência em gestão de operações com múltiplos stakeholders.Experiência com centros de referência e linhas de cuidado para pacientes com doenças raras. #LI-CES #LI-DNP #LI-LATAM IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

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    Vaga PCD Consultor Navegador (Pessoa Com Deficiência - PCD)

    IQVIA
    São Paulo - SP

    Somente PCD - Missão do Cargo Realizar o acompanhamento de pacientes e cuidadores ao longo da jornada de cuidado, promovendo acolhimento, orientação operacional e articulação entre os diferentes envolvidos no processo. Atuar na identificação e no suporte à resolução de barreiras administrativas, documentais, logísticas e de comunicação que possam impactar o acesso e a continuidade do cuidado, garantindo o cumprimento dos fluxos e processos estabelecidos. Principais Responsabilidades Acolher pacientes e cuidadores, prestando orientações claras sobre as etapas da jornada.Realizar acompanhamento contínuo dos pacientes conforme fluxos e protocolos definidos.Apoiar o agendamento e a coordenação de consultas, avaliações, procedimentos e demais etapas previstas no processo.Apoiar a coordenação logística necessária para garantir a continuidade da jornada de cuidado.Identificar e direcionar barreiras administrativas, documentais, logísticas, geográficas ou de comunicação aos responsáveis adequados.Monitorar pendências, cancelamentos, reagendamentos e riscos de descontinuidade do acompanhamento.Apoiar a gestão da documentação necessária ao processo, respeitando os limites de atuação do cargo.Atuar como ponto focal operacional entre pacientes, cuidadores, equipes assistenciais, instituições e prestadores de serviço.Apoiar treinamentos sobre fluxos operacionais, registros e responsabilidades utilizando materiais aprovados.Registrar interações, acompanhamentos, ocorrências e encaminhamentos nos sistemas definidos, assegurando qualidade e rastreabilidade das informações.Apoiar a consolidação de dados e indicadores operacionais.Participar de reuniões, treinamentos, auditorias e iniciativas de melhoria contínua.Reportar desvios, incidentes, situações críticas e demandas fora do escopo aos responsáveis pela gestão da operação. Qualidade, Segurança da Informação e Conformidade Seguir procedimentos, fluxos, treinamentos e controles de qualidade estabelecidos.Identificar e encaminhar relatos recebidos durante as interações, de acordo com os procedimentos definidos.Não realizar avaliações, diagnósticos ou classificações técnicas de relatos recebidos.Garantir a confidencialidade e o tratamento adequado de dados pessoais e informações sensíveis.Utilizar apenas sistemas, equipamentos e canais aprovados.Comunicar imediatamente qualquer suspeita de incidente de privacidade, falha de processo ou não conformidade.Participar de atividades de auditoria, monitoramento e verificação de qualidade, quando aplicável. Formação e Experiência Requisitos Ensino superior completo na área da saúde.Formação preferencial em Enfermagem, Farmácia ou Serviço Social.Conhecimento do sistema de saúde público e privado.Conhecimento de fluxos de acesso e navegação em saúde.Experiência com atendimento, orientação ou acompanhamento de pacientes.Habilidade de relacionamento com pacientes, cuidadores e profissionais de saúde.Conhecimento do Pacote Microsoft Office e ferramentas de registro.Disponibilidade para atuação em campo e deslocamentos, quando necessário.Conhecimento sobre doenças raras e suas jornadas de cuidado.Disponibilidade para viagens frequentes.CNH categoria B válidaVeículo próprio em boas condiçõesSeguro vigente. Importante: Esta posição envolve atividades externas que requerem deslocamentos frequentes para atendimento a clientes e visitas técnicas. Por isso, é indispensável que o(a) candidato(a) possua veículo próprio, Carteira Nacional de Habilitação (CNH) válida e documentação do veículo regularizada. Na etapa final do processo seletivo, será realizada a validação documental, com a solicitação do envio das seguintes cópias: CNH (Carteira Nacional de Habilitação);CRLV (Certificado de Registro e Licenciamento do Veículo);Comprovante de seguro.A participação nesta etapa é obrigatória para a continuidade no processo. Diferenciais Experiência em programas de acompanhamento e suporte ao paciente.Experiência com centros de referência e linhas de cuidado para pacientes com doenças raras.Experiência em coordenação de jornadas assistenciais e acesso ao tratamento.#LI-CES #LI-DNP #LI-LATAM IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

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    Vaga PCD RWE - Site Mgr 2 (Pessoa Com Deficiência - PCD)

    IQVIA
    São Paulo - SP

    Somente PCD - Job OverviewWith limited guidance, responsible for remote site monitoring activities to ensure sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements. May monitor and/or co-monitor on-site when needed. May perform Site Identification (Site ID) and/or Site Start-Up (SSU) activities. Essential Functions• Completes appropriate therapeutic, protocol and clinical research training to perform job duties. Works collaboratively with other functional groups such as Clinical Operations Lead (COL), Project Management, Regulatory Start-Up (RSU) and Epidemiology.• Performs as needed, Site ID, and site selection activities according to applicable regulations and Standard Operating Procedures (SOPs) including but not limited to: Collection of Site Information Form (SIF) and Confidentiality Disclosure Agreement (CDA) and corresponding tracking and filing and might perform Site Selection Visits (SSVs) as needed.• Performs as needed SSU activities according to applicable regulations and SOPs, including but not limited to: preparing regulatory/ethics submission packages and obtaining required approvals; collecting and reviewing of regulatory documents for completeness and accuracy; tracking and filing site regulatory documents (Including regulatory /ethics submissions / Approvals, Informed Consent Form (ICF) and others), preparing, reviewing and negotiating of site contracts and budgets with investigator sites; reviewing and agreeing on project planning and project timelines.• Performs as needed, initiation, monitoring and close out visits remotely and in accordance with contracted scope of work, using Good Clinical Practices (GCP), applicable regulations, SOPs and work instructions. May monitor and/or co-monitor on-site when needed.• Serves as primary contact between the business and the investigator site and ensures proper documentation of site management communications. Serves as back-up to other Site Managers (SMs).• In collaboration with the assigned field Clinical Research Associates (CRAs), performs routine site management activities, including, as needed: SSU activities as detailed above, site training, assistance with site questions, patient recruitment and retention management, study supplies management, and other activities needed to ensure that assigned sites are conducting the study(ies) as required by the study protocol, applicable regulations and guidelines, and sponsor requirements.• Collaborates with field CRAs, as needed, to resolve and document outstanding site issues/action items.• Reviews the quality and integrity of patient data at assigned sites through the remote review of electronic Case Report Form (CRF) data. Ensures timely transmission of clinical data from assigned study sites and works with sites to resolve data queries.• Assists with final data review, query resolution and patient casebook signature through database lock. Inclusive of patient profile and data listings review.• Ensures accurate completion and maintenance of internal systems, databases and tracking tools with site specific information, including (but not limited to) submitting regular visit reports, generating follow-up letters, collection and filing of essential documents and other required study documentation.• Provides input and updates to the assigned COL regarding site status and deliverables. Escalate issues and/or risks related to site performance to the COL, Clinical Project Manager (CPM) and/or Line Manager (LM) as needed.• May assist with and attend (as needed) Investigator Meetings on assigned studies.• Authorized to request onsite visits and/or site audits for reasons of validity.• May help ensure timely and appropriate site payments and updates to systems as required to ensure proper timing and amount of payments.• May conduct assessment visits, as needed, to ensure monitoring is being conducted in accordance with the protocol, SOPs, GCP and applicable regulatory requirements.• May provide assistance to less experienced clinical staff, including demonstrating appropriate interactions with sites, documentation and other monitoring activities.• May be assigned COL tasks on exceptional basis, as agreed with LM. Qualifications• Bachelor's Degree Bachelor's Degree preferred or as required by local country policies. Degree in scientific discipline or health care preferred. Pref• Minimum of 2 plus years of relevant clinical experience preferred. Pref• Equivalent combination of education, training and experience may be acceptable. Pref• Intermediate knowledge of clinical research process and medical terminology.• Written and verbal communication skills including good command of English language.• Good organizational and problem-solving skills.• Ability to manage multiple priorities within various clinical trials.• Ability to meet deadlines and adhere to project timelines.• Ability to work independentl

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    Vaga PCD PMO – Project Manager (Pessoa Com Deficiência - PCD)

    IQVIA
    São Paulo - SP

    Somente PCD - Sobre a posição Responsável por garantir a governança, padronização e acompanhamento dos projetos da área de Educação Médica Latam (AMI), assegurando alinhamento com as estratégias corporativas e compliance regulatório. Atua como facilitador entre equipes de tecnologia, áreas de negócio e stakeholders, promovendo boas práticas de gestão de projetos e eficiência operacional. Principais Responsabilidades Implementar e manter frameworks de governança para gestão de projetos, iniciativas de aprendizagem e otimização de processos da área AMI. Acompanhar cronogramas, escopo, orçamento, riscos e indicadores dos projetos, garantindo qualidade das entregas e cumprimento dos prazos. Desenvolver e consolidar relatórios executivos, dashboards e KPIs para suporte à tomada de decisão. Apoiar a gestão e priorização do portfólio de projetos, alinhando recursos, demandas e estratégias organizacionais. Garantir aderência às políticas corporativas, requisitos regulatórios e normas de compliance da indústria farmacêutica. Facilitar a comunicação entre equipes técnicas, áreas de negócio, fornecedores e stakeholders internos. Planejar e conduzir reuniões de governança, comitês executivos e ritos de acompanhamento dos projetos. Identificar oportunidades de melhoria contínua, eficiência operacional e padronização de processos. Atuar como ponto focal para interação com a matriz global e afiliadas da América Latina, assegurando alinhamento das iniciativas regionais. Requisitos Ensino superior completo em Administração, Engenharia, Tecnologia da Informação, Gestão de Projetos, Ciências da Saúde ou áreas correlatas. Pós-graduação ou especialização em Gestão de Projetos será considerada um diferencial. Experiência sólida em gestão de projetos e/ou atuação em PMO. Vivência em governança de projetos, gestão de portfólio e indicadores de performance. Experiência em ambientes corporativos complexos e com múltiplos stakeholders. Desejável experiência em empresas farmacêuticas, healthcare, life sciences ou áreas de educação médica. Gestão de riscos, cronogramas, orçamento e controle de indicadores. Ferramentas de gestão de projetos e visualização de dados (MS Project, Smartsheet, Jira, Power BI, entre outras). Conhecimento de processos de compliance e ambiente regulado será considerado um diferencial. Idiomas Inglês avançado para comunicação com equipes globais e matriz. Espanhol intermediário ou avançado será considerado um diferencial importante. Capacidade de atuar em ambiente multicultural e regional LATAM. Competências Comportamentais Organização e atenção aos detalhes. Forte capacidade analítica e visão de processos. Comunicação clara e influência sem autoridade formal. Proatividade e senso de dono. Capacidade de priorização e gestão de múltiplos projetos simultaneamente. Relacionamento interpessoal e colaboração. Perfil orientado a resultados e melhoria contínua. A IQVIA está empenhada em adotar um ambiente de trabalho diverso e inclusivo. Nosso objetivo é atrair e reter as melhores pessoas, independentemente de gênero, raça, estado civil, origem étnica, nacionalidade, idade, deficiência, orientação sexual, identidade de gênero ou qualquer outra característica. Junte-se a nós! ⚠️A IQVIA realiza contato com candidatos exclusivamente por meio de seus canais oficiais de recrutamento, incluindo e-mails corporativos com domínio @iqvia.com e plataformas de seleção autorizadas pela empresa. Caso receba uma comunicação suspeita em nome da IQVIA por canais não oficiais, recomendamos que não compartilhe informações pessoais e entre em contato conosco pelos canais oficiais para verificação. #LI-CES #LI-DNP #LI-LATAM IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

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    Vaga PCD Site Activation Specialist (Pessoa Com Deficiência - PCD)

    IQVIA
    São Paulo - SP

    Somente PCD - Under moderate supervision, executes the feasibility, site identification regulatory, start-up, and maintenance activities in accordance with regulations, SOPs, and project requirements at the regional, or country level. Prepares and manages site documentation; reviews and negotiates site documents and contracts with sites and sponsors; maintains, reviews, and reports on site performance metrics; serves as the primary point of contact for investigative sites; tracks completion of appropriate documents for sites; ensures contracts are fully executed; and establishes project timelines. With moderate oversight and supervision, perform tasks at a country/region level associated with site activation activities in accordance with applicable local and/or internationalregulations, standard operating procedures (SOPs), project requirements and contractual/budgetary guidelines. May also include maintenance activities. Essential Functions • With moderate oversight and supervision, werve a Single Point of Contact (SPOC) to perform feasibility, site activation and some maintenance activities in assigned studies for investigative sites, according to applicable regulations, SOPs and work instructions, working closely with the Site Activation Manager (SAM), Project Management team, and other departments as necessary. Review documents for completeness, consistency and accuracy, under guidance of senior staff.• Prepare site documents, reviewing for completeness and accuracy.• Inform team members of completion of regulatory contractual. and other documents for individual sites.• Distribute completed documents to sites and internal project team members.• Update and maintain internal systems, databases, tracking tools, timelines and project plans with accurate and complete project specific information.• Review, track and follow up the progress, the approval and execution of required documents such as questionaires, CDAs, regulatory, ethics, Informed Consent Form (ICF) and Investigator Pack (IP) release documents. Requires advanced knowledge within a specific discipline typically gained through extensive work experience and/or education. Qualifications • Bachelor's Degree Life sciences or a related field Req And• Other 1 - 3 years’ clinical research or other relevant experience; or equivalent combination of education, training and experience. Req• With 3 years’ experience in a healthcare environment or equivalent combination of education, training and experience. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

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    Vaga PCD Revenue Analyst (Pessoa Com Deficiência - PCD)

    IQVIA
    São Paulo - SP

    Somente PCD - The Revenue Analyst supports revenue realization and collections activities across a portfolio of large global pharmaceutical customers. This role is responsible for managing customer accounts, researching invoice and payment issues, resolving billing disputes, and driving timely cash collection. The successful candidate will act as a key liaison between customers and internal business partners to troubleshoot complex issues, remove payment barriers, and ensure efficient revenue recovery. The position requires strong analytical skills, exceptional organization, effective communication, and the ability to manage a high-volume portfolio in a fast-paced global environment. Key Responsibilities Manage a portfolio of approximately 10 to 20 large pharmaceutical customer accounts. Monitor aging reports, outstanding balances, payment trends, and collection performance. Investigate and resolve invoice disputes, payment delays, purchase order discrepancies, and billing-related issues. Collaborate with Billing, Project Finance, Operations, Sales, and customer stakeholders to drive issue resolution. Build strong working relationships with customers while managing challenging conversations professionally and effectively. Support monthly cash collection targets and revenue realization objectives. Maintain accurate account documentation, follow-up activities, and collection records. Prepare reports and perform analysis to support customer reviews and business decisions. Identify process improvement and automation opportunities to enhance operational efficiency. Serve as a facilitator between internal and external stakeholders to ensure timely payment approval and issue resolution. Demonstrated ability to influence stakeholders, negotiate payment solutions, and manage difficult customer conversations. Ability to work independently, prioritize activities, and drive complex issues to resolution with limited supervision. English communication skills (written and verbal) required, with the ability to interact effectively with global customers and stakeholders. Requirements Bachelor's degree in Finance, Business Administration, Economics, Accounting, or related field. Previous experience in Accounts Receivable, Collections, Billing, Customer Financial Services, Revenue Operations, Finance, or related areas preferred. Strong analytical and problem-solving skills. Proven ability to manage multiple priorities and large volumes of information simultaneously. Excellent verbal and written communication skills. Customer-focused mindset with strong stakeholder management capabilities. Advanced organizational and follow-up skills. Strong Excel skills, including data analysis and reporting. Experience with Microsoft Office applications. Experience with ERP systems such as PeopleSoft is a plus. Experience with Salesforce, CRM platforms, process improvement initiatives, or automation projects is highly desirable. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

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    Vaga PCD Site Activation Specialist (North America team) (Pessoa Com Deficiência - PCD)

    IQVIA
    São Paulo - SP

    Somente PCD - Job OverviewUnder moderate supervision, executes the feasibility, site identification regulatory, start-up, and maintenance activities in accordance with regulations, SOPs, and project requirements at the regional, or country level.Prepares and manages site documentation; reviews and negotiates site documents and contracts with sites and sponsors; maintains, reviews, and reports on site performance metrics; serves as the primary point of contact for investigative sites; tracks completion of appropriate documents for sites; ensures contracts are fully executed; and establishes project timelines. With moderate oversight and supervision, perform tasks at a country/region level associated with site activation activities in accordance with applicable local and/or international regulations, standard operating procedures (SOPs), project requirements and contractual/budgetary guidelines. May also include maintenance activities.Essential Functions• With moderate oversight and supervision, serve a Single Point of Contact (SPOC) to perform feasibility, site activation and some maintenance activities in assigned studies for investigative sites, according to applicable regulations, SOPs and work instructions, working closely with the Site Activation Manager (SAM), Project Management team, and other departments as necessary. Review documents for completeness, consistency and accuracy, under guidance of senior staff.• Prepare site documents, reviewing for completeness and accuracy.• Inform team members of completion of regulatory contractual. and other documents for individual sites.• Distribute completed documents to sites and internal project team members.• Update and maintain internal systems, databases, tracking tools, timelines and project plans with accurate and complete project specific information.• Review, track and follow up the progress, the approval and execution of required documents such as questionaires, CDAs, regulatory, ethics, Informed Consent Form (ICF) and Investigator Pack (IP) release documents. Requires advanced knowledge within a specific discipline typically gained through extensive work experience and/or education.Qualifications• Based in Argentina or Brazil.• Bachelor's Degree Life sciences or a related field required.• Other 1 - 3 years’ clinical research supporting site activation/regulatory tasks.• Advanced level of English. You will be working with a team from the US and interacting with North American sites. Please, make sure to submit your CV in English. It will be assessed by a global team. ⚠️ IQVIA contacts candidates exclusively through its official recruitment channels, including corporate email addresses ending in @iqvia.com and company-authorized recruitment platforms. If you receive a suspicious communication claiming to be from IQVIA through unofficial channels, we recommend that you do not share any personal information and contact us through our official channels for verification. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

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    Vaga PCD Sr. CRA 1, Brazil (Pessoa Com Deficiência - PCD)

    IQVIA
    São Paulo - SP

    Somente PCD - IQVIA Biotech is now hiring for Sr. CRA 1 location Brazil, oncology preferred. IQVIA Biotech is a full-service CRO purpose-built to serve biotech sponsors. With over 25 years of experience, we offer agile, therapeutically aligned solutions and trusted partnerships that help bring breakthrough treatments to patients faster. Job Profile Summary: Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements. Essential Job Functions, Duties and Responsibilities: • Perform site monitoring visits (selection, initiation, monitoring, and close-out visits) in accordance with contracted scope of work and Good Clinical Practice. • Work with sites to adapt, drive, and track subject recruitment plan in line with project needs to enhance predictability. • Administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issues. • Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations. Escalate quality issues as appropriate. • Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (CRF) completion and submission, and data query generation and resolution. May support start-up phase. • Ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File (ISF) is maintained in accordance with GCP and local regulatory requirements. • Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters and other required study documentation. • Collaborate and liaise with study team members for project execution support as appropriate. Responsibilities Essential Functions • If applicable, may be accountable for supporting development of project subject recruitment plan on a per site basis. • If applicable, may be accountable for site financial management according to executed clinical trial agreement and retrieve invoices according to local requirement. Qualifications • Bachelor's Degree in scientific discipline or health care preferred. • Requires at least 3-4 years of year of on-site monitoring experience. • Equivalent combination of education, training and experience may be accepted in lieu of degree. • Good knowledge of, and skill in applying, applicable clinical research regulatory requirements. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

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    Vaga PCD Associate Study Start Up Manager (Pessoa Com Deficiência - PCD)

    IQVIA
    São Paulo - SP

    Somente PCD - Job OverviewDirect and manage the delivery of all required site activation, maintenance and regulatory activities for selected studies or multi-protocol programs, including pre-award activities, oversight of the scope of work, budget and resources. Essential Functions• Oversee the execution of Site Activation (including pre-award/bid defense activities) and/or Maintenance for assigned projects in accordance with the agreed RSU site activation strategy, adhering to project timelines. Develop, implement and maintain the Management Plan according to the Scope of Work and Project Plan, within the agreed project strategy, resolving project related issues where required. Ensure collaboration across Regulatory & Site Activation, including communication with regions and countries, to successfully deliver the agreed project scope in compliance with the RSU Management Plan. Create and/or review technical and administrative documentation to support business development and enable study initiation and maintenance, as required. Provide specialist regulatory and technical scientific support to facilitate efficient business development, initiation and maintenance of clinical trials, whilst enabling compliance with regulatory requirements. Provide overall guidance and oversight of multi-regional and multi-protocol programs during initial start-up and maintenance phase as an integral member of the study management team. Determine regulatory strategy/expectations and parameters for submissions and all necessary authorizations• identify regulatory complexity and challenges and offer creative and practical solutions to support the bid process and subsequent execution of the site activation plan. Assess and review the regulatory landscape and contribute to the collection, interpretation, analysis and dissemination of accurate regulatory intelligence to support assigned studies and wider company, as required. Execute operational strategy/ expectations for maintenance of clinical study approvals, authorizations and review/ negotiation of contracts and essential documents. Work with Quality Management to ensure appropriate quality standards for the duration of site activation (or Maintenance, as applicable). Mentor and coach colleagues as required. Ensure accurate completion and maintenance of internal systems (with emphasis on CTMS), databases, tracking tools, timelines and project plans with project specific information. May take a lead role in developing long standing relationships with preferred IQVIA customers. Deliver presentations/training to clients, colleagues and professional bodies, as required. May be involved in activities related to monthly study budget planning and reviews. Qualifications• Bachelor's Degree Life sciences or related field Req• 7 years’ relevant experience in a scientific or clinical environment including demonstrable experience in an international role. Equivalent combination of education, training and experience.• Strong negotiation and communication skills with ability to challenge• Excellent interpersonal skills and strong team player• Proven ability to work through others to deliver results to the appropriate quality and timeline metrics on complex projects• Thorough understanding of regulated clinical trial environment and in depth knowledge of drug development process• Demonstrated proficiency in using systems and technology to achieve work objectives• Good regulatory and/or technical writing skills• Strong knowledge and ability to apply Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines and applicable regulatory guidelines• Good leadership skills, with ability to motivate, coach and mentor• Good organizational and planning skills• Ability to exercise independent judgment taking calculated risks when making decisions• Good presentation skills• Proven ability to establish and maintain effective working relationships with co-workers, managers and sponsors.• Excellent understanding of study financial management• Proven ability to work on multiple projects balancing competing priorities IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and profess

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    Vaga PCD Talent Acquisition Assistant (Exclusive for People with Disabilities) (Pessoa Com Deficiência - PCD)

    IQVIA
    São Paulo - SP

    Somente PCD - This is a talent pool for people with disabilities. If you do not belong to this group and wish to apply, you can apply for other vacancies within IQVIA jobs. Job Overview IQVIA is committed to fostering an inclusive workplace where diversity drives innovation. This opportunity is exclusively intended for People with Disabilities (PwD). Location: São Paulo, BrazilWork Model: HybridEmployment Type: Full-time As a Talent Acquisition Assistant, you will support recruitment activities across Latin America, partnering with recruiters and stakeholders to ensure a positive candidate experience and efficient hiring processes. The role combines recruitment coordination, talent market insights, sourcing support, and administrative activities. Key Responsibilities Support recruitment operations and maintain accurate candidate data and reports.Gather talent market insights and feedback from new hires across LATAM, with a focus on Brazil.Coordinate interviews and manage scheduling between candidates and hiring teams.Support candidate sourcing initiatives through LinkedIn and other recruiting channels.Assist with job posting, employer branding, and talent attraction activities.Provide general administrative support to the Talent Acquisition team. Qualifications Bachelor's degree in Human Resources, Psychology, Business Administration, Communications, or a related field.Previous experience in recruitment, talent acquisition coordination, administration, or customer-facing support roles is a plus.Strong organizational skills and attention to detail.Experience working with MS Office, ATS platforms or LinkedIn is preferred.Intermediate level of English and/or Spanish.Strong communication and teamwork skills. Inclusion Statement IQVIA is an equal opportunity employer and is committed to creating an inclusive environment for all employees. This position is exclusively intended for People with Disabilities (PwD). If you require accommodations during the recruitment process, please indicate your needs when applying. All information will be handled confidentially and in accordance with applicable regulations IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

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    Vaga PCD Centralized Monitoring Lead in LATAM (Remote) (Pessoa Com Deficiência - PCD)

    IQVIA
    São Paulo - SP

    Somente PCD - Job Overview The Leader of the Centralized Monitoring team, partner with the project and clinical lead to achieve the delivery of the project’s overall objectives to the sponsor’s satisfaction per contract, while optimizing speed, quality and cost of delivery and in accordance with IQVIA SOPs, policies and practices. Essential Functions: Leadership activities: Leader of the Centralized Monitoring team, partner with the project and clinical lead to perform oversight on clinical deliverables on global assigned projects as per the protocol, SOPs, respective regulation/guidelines and project Clinical Operations Plan. Unblinded Clinical Lead, including IP management for the assigned study to identify risk and proposed mitigation (including re-supply, re-labelling, Import/export licenses etc.) May act as Clinical Lead when there is not assigned to the study and at project close out. Manage project resources (CRAs/ Central Monitors/ Clinical Trial Assistants/ Centralized Monitoring Assistants) Analytical activities: Manage, monitor and complete study/site metrics trending (trend analysis of clinical aspects of the trial, share trends and agree on action plan, review, triage and action clinical study alerts, monitor clinical operation plan compliance etc.). Contribute to developing the study specific analytics strategy and work on developing advanced analytics. Support project management team to develop monitoring strategy, including monitoring triggers/thresholds. Attend study team and /or client meetings. Provide Inputs to clinical study teams, key decision makers, and internal team members to manage continuous process improvements, issue escalation, workload projections. Development and use of study management plans, and/or RBM specific tools and templates, and/or other study specific plans to evaluate the quality and integrity of the study. Ensure complete and accurate documentation of all the study specific tools and templates and keep the project Audit ready, including eTMF oversight. Mentors or coaches for junior staff. Qualifications: Bachelor's degree in life sciences or related field. +3 years of relevant clinical monitoring experience (as remote or on site CRA). Advanced knowledge of clinical trial conduct and skill in applying applicable clinical research regulatory requirements; i.e., ICH GCP and relevant local laws, regulations and guidelines, towards clinical trial conduct. +2 years in a Lead role. Strong written and verbal communication skills including advanced command of English (Mandatory). Strong organizational, problem solving and decision making skills. Results and detail-oriented approach to work delivery and output. Excellent motivational, influencing, negotiating and coaching skills. Ability to work on multiple global projects and manage competing priorities. To lead team and effectively work in team. #LI-NRJ #LI-Remote IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

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    Vaga PCD AI Engineer (Pessoa Com Deficiência - PCD)

    IQVIA
    São Paulo - SP

    Somente PCD - Role Summary We are seeking a highly skilled Senior Consultant - AI Engineer to design, develop, and deploy scalable AI-powered solutions that address complex commercial, medical, and patient-centric challenges in the Healthcare and Life Sciences industry. This role combines advanced AI engineering, machine learning, Generative AI, Agentic AI, and healthcare analytics expertise to create innovative, production-grade solutions that drive measurable business value. The ideal candidate will have strong experience in building enterprise AI applications, LLM-based solutions, intelligent agents, and modern analytics platforms while working with healthcare datasets such as claims, prescription, EMR/EHR, real-world data (RWD), CRM, patient support, clinical, and scientific data. This individual will partner closely with business stakeholders, methodologists, data scientists, and technology teams to translate business problems into scalable AI solutions, reusable accelerators, and intellectual property. Key Responsibilities AI Solution Development & Engineering Design, build, deploy, and maintain production-grade AI and machine learning solutions across commercial, medical, and patient analytics use cases. Develop enterprise-scale Generative AI and Agentic AI applications leveraging Large Language Models (LLMs). Build Retrieval-Augmented Generation (RAG) architectures, semantic search systems, knowledge agents, and intelligent workflow automation solutions. Create reusable AI frameworks, APIs, accelerators, and platform components that can be deployed across multiple clients and therapeutic areas. Develop scalable AI orchestration frameworks using agent-based architectures and workflow management tools. AI Platform & MLOps Engineering Develop cloud-native AI solutions using modern AI development platforms and frameworks. Implement software engineering best practices including CI/CD, version control, automated testing, observability, and monitoring. Establish AI deployment pipelines for model operationalization, monitoring, governance, and performance optimization. Ensure scalability, security, reliability, and compliance of AI solutions in regulated healthcare environments. Collaborate with data engineering teams to build robust data pipelines and AI-ready data ecosystems. Generative AI & Agentic AI Design and implement: Large Language Model (LLM) applications Retrieval-Augmented Generation (RAG) systems Semantic search solutions Prompt engineering frameworks AI agents and multi-agent systems Workflow orchestration platforms Evaluate, validate, and benchmark AI models to ensure accuracy, reliability, explainability, and business relevance. Contribute to AI governance, Responsible AI practices, and model risk management frameworks. Healthcare Analytics & Business Impact Apply AI and advanced analytics to solve Healthcare and Life Sciences challenges using: Claims data Prescription data EMR/EHR data Real-World Data (RWD) Commercial and CRM data Patient support data Clinical and scientific data Develop AI-enabled solutions that improve commercial effectiveness, customer engagement, forecasting accuracy, patient outcomes, and decision support. Partner with healthcare domain experts to ensure solutions align with industry needs and regulatory expectations. Stakeholder Management & Consulting Translate ambiguous business challenges into structured AI and analytics solutions. Engage with business leaders, clients, methodologists, and cross-functional teams to define solution roadmaps and implementation strategies. Present technical concepts and AI insights in a manner that is understandable to executive and non-technical audiences. Mentor junior engineers and contribute to building organizational AI capabilities and best practices. Support thought leadership initiatives and contribute to AI innovation within the organization. Must-have requirements: 2-6 years of experience building and deploying AI/ML solutionsHands-on experience with Generative AI, LLMs, and RAGExperience with Agentic AI, semantic search, and AI workflow orchestrationStrong Python and SQL skillsExperience with Databricks, Snowflake, Spark/PySpark, and cloud platforms (Azure, AWS, or GCP)Experience building APIs, scalable AI services, and enterprise AI applicationsKnowledge of MLOps/LLMOps, CI/CD, Docker/Kubernetes, Git, and model deploymentHealthcare/Life Sciences experience, including claims, EMR/EHR, RWD, prescription, clinical, or CRM dataStrong stakeholder management, consulting, and communication skillsAbility to translate business problems into scalable AI solutions and mentor junior team members IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and populat

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    Vaga PCD Project Manager (Data as a Service) (Pessoa Com Deficiência - PCD)

    IQVIA
    São Paulo - SP

    Somente PCD - OverviewThe Project Manager is responsible for managing end-to-end client data delivery projects using IQVIA's Data as a Service (DaaS) platform. This role serves as the primary point of contact for internal and external stakeholders, ensuring projects are delivered on time, within scope, and aligned with client expectations. ResponsibilitiesManage multiple concurrent client data delivery projects from initiation through production and support transition. Lead project kickoffs, client meetings, and day-to-day stakeholder communication. Define requirements, track deliverables, and coordinate Technical Leads and Configurators. Develop and maintain project plans, timelines, status reports, and project documentation. Identify risks, manage escalations, and drive issue resolution. Monitor project budgets, pricing, and deliverables tied to revenue milestones. Ensure compliance with standard processes, quality requirements, and best practices. Provide project updates to leadership and participate in process improvement initiatives. Support proposal development, change orders, and scope management activities. Required QualificationsExperience in project coordination or project management, preferably within technology or data-driven environments. Understanding of database concepts, SQL, ETL processes, and data delivery solutions. Familiarity with Snowflake, Databricks, and Redshift environments. Strong organizational, analytical, and problem-solving skills. Ability to manage multiple workstreams in a fast-paced environment. Excellent stakeholder management and communication skills. English proficiency at C1+ level. Preferred QualificationsPrevious IT Project Management experience. Knowledge of pharmaceutical data and healthcare datasets. Experience working with client-facing projects and cross-functional teams. Additional InformationClient-facing role with frequent interaction with internal and external stakeholders. Fast-paced environment, managing approximately 20 active client deliveries simultaneously. EST business hours coverage required (8:00 AM – 5:00 PM EST). Occasional flexibility outside standard hours to support client delivery needs. Ideal CandidateA project-oriented professional who combines strong stakeholder management skills with a solid understanding of databases and data platforms, and who thrives in a high-volume, customer-focused delivery environment. ⚠️ IQVIA contacts candidates exclusively through its official recruitment channels, including corporate email addresses ending in @iqvia.com and company-authorized recruitment platforms. If you receive a suspicious communication claiming to be from IQVIA through unofficial channels, we recommend that you do not share any personal information and contact us through our official channels for verification. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

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    Vaga PCD CRA 2, Brazil (Pessoa Com Deficiência - PCD)

    IQVIA
    São Paulo - SP

    Somente PCD - IQVIA Biotech is now hiring for CRA 2 with a minimum of 1 year of on-site monitoring in oncology. IQVIA Biotech is a full-service CRO purpose-built to serve biotech sponsors. With over 25 years of experience, we offer agile, therapeutically aligned solutions and trusted partnerships that help bring breakthrough treatments to patients faster. Job OverviewWe are seeking a dedicated Clinical Research Associate (CRA) to join our team and play a key role in ensuring the successful execution of clinical trials. In this position, you will be responsible for monitoring and managing clinical sites to ensure compliance with study protocols, regulatory requirements, and sponsor expectations. Your work will directly contribute to the integrity and quality of clinical research data. Key Responsibilities Conduct all types of site visits—selection, initiation, monitoring, and close-out in alignment with the contracted scope of work, Good Clinical Practice (GCP), and ICH guidelines. Collaborate with site staff to implement and track subject recruitment strategies that align with project timelines and enrollment goals. Deliver protocol and study-specific training to site personnel and maintain consistent communication to manage expectations and resolve issues. Assess site performance and adherence to the protocol, escalating quality concerns as needed to ensure compliance and data integrity. Monitor study progress by tracking regulatory submissions, subject enrollment, case report form (CRF) completion, and resolution of data queries. Ensure that essential documents are collected and maintained in both the Trial Master File (TMF) and the Investigator Site File (ISF) in accordance with regulatory standards. Document site management activities, visit outcomes, and follow-up actions through detailed reports and correspondence. Work closely with cross-functional project teams to support study execution and ensure alignment with project goals. Depending on the project, you may also support site-level recruitment planning and financial management, including invoice collection and budget tracking. Qualifications Bachelor’s degree in life sciences or health-related field (or equivalent experience). Requires at least 1 year of on-site monitoring experience. Strong understanding of GCP, ICH guidelines, and regulatory requirements. Ability to travel as required by the project. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

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    Vaga PCD Sr.CRA 1 (Pessoa Com Deficiência - PCD)

    IQVIA
    São Paulo - SP

    Somente PCD - Location: Brazil (Sao Paulo) About Us: Join our team and help shape the future of our organization. We are a leading company committed to excellence and innovation, seeking a talented Senior Recruiter to support our growth. Job Overview: Manage a team of clinical staff working in support of clinical studies to ensure projects are appropriately resourced and employees are trained and meeting project objectives. Key Responsibilities: Manage staff in accordance with organization’s policies and applicable regulations. Responsibilities include planning, assigning, and directing work, assessing performance and guiding professional development, rewarding and disciplining employees, and addressing employee relations issues and resolving problems. Participate in the selection for hiring new employees by conducting candidate review and participating in the interviewing process. Ensure that new employees are properly onboarded and trained. Ensure that staff has the proper materials, systems access and training to complete job responsibilities. Provide oversight for the execution of the training plan, SOP review and training experiences, as applicable. Participate in the allocation of resources to clinical research projects by assigning staff to clinical studies based on their experience and training. Manage the quality of assigned staff's clinical work through regular review and evaluation of work product. Identifies quality risks and issues and create appropriate corrective action plans to prevent or correct deficiencies in performance of staff. Ensures that staff are meeting defined workload and quality metrics through regular review and reporting of findings as outlined by clinical operations management. May collaborate with other clinical teams and other functional leadership to manage project related challenges and to achieve exemplary customer service. Participates in corporate or organizational departmental quality or process improvement initiatives. Basic Qualifications: Bachelor's Degree Degree in scientific discipline or health care preferred. Pref Prior clinical trial experience including experience in a management/leadership capacity or equivalent combination of education, training and experience. In-depth knowledge of applicable clinical research regulatory requirements (i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines). Others requirements: Strong attention to detail and excellent communication skills. Good leadership skills. Exceptional problem-solving, judgment, and decision-making abilities. Computer skills including proficiency in use of Microsoft Word, Excel and PowerPoint and use of a laptop computer and iPhone and iPad (where applicable). Written and verbal communication skills including good command of English language. Organizational and problem-solving skills. Effective time and financial management skills. Ability to establish and maintain effective working relationships with coworkers, managers, and clients. Why Join Us? Be part of an innovative and forward-thinking company that collaborates to make a healthier world. Work alongside a diverse and talented team. Many opportunities for professional growth by developing project mgmt abilities. Competitive salary and benefits package. IQVIA is committed to embracing a diverse and inclusive work environment. Our goal is to attract and retain the best people, regardless of their gender, race, marital status, ethnic origin, national origin, age, disability, sexual orientation, gender identity or any other characteristic. Join us! IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

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    Vaga PCD Consultor Técnico (Pessoa Com Deficiência - PCD)

    IQVIA
    São Paulo - SP

    Somente PCD - Visão geral do trabalho Maximizar o crescimento das vendas em um território geográfico específico, de acordo com a estratégia e os objetivos da empresa. Funções essenciais •Realizar visitas a médicos e outros profissionais importantes na estrutura decisória de hospitais e outras instituições de saúde. •Realizar e gerenciar todo o processo de vendas dos produtos com os quais trabalha nos hospitais e outras instituições de saúde de seu painel. •Organizar eventos com médicos e outros profissionais da hospitais e instituições de saúde visitadas, sempre respeitando a legislação pertinente do país. •Acompanhar e analisar resultados, implementando ações para o atingimento das metas estabelecidas. • Manter registros atualizados no sistema de CRM. • Informar sobre atividades dos concorrentes e outras mudanças no mercado. • Manter conhecimento técnico/comercial atualizado nas áreas de especialidade. • Manter todos os equipamentos da empresa seguros e em bom estado de conservação. • Compartilhar experiências, ideias e técnicas para auxiliar no treinamento de vendas. • Assegurar a notificação de quaisquer Eventos Adversos identificados de acordo com o processo e as diretrizes vigentes, relatando para a Farmacovigilância. Qualificações • Ensino superior completo; • Experiência com mercado oncológico (obrigatório); • Experiência no segmento hospitalar (obrigatório); • Experiência em Acesso Privado (diferencial); • Experiência prévia com medicamentos biológicos; • Fluência em sistemas operacionais de software, como MS Office e sistemas de gerenciamento de relacionamento com clientes; • Capacidade de estabelecer e manter relacionamentos de trabalho eficazes com colegas de trabalho, gerentes e clientes; • CNH – Válida; • Veículo próprio para uso durante as atividades profissionais; • Disponibilidade para viagens; Localidade de atuação: Rio de Janeiro/RJ e São Paulo/SP Importante: Esta posição exige que o(a) candidato(a) possua carro próprio, CNH válida e documentação do veículo em dia. Como parte do processo seletivo, haverá uma etapa final de validação documental, na qual será solicitado o envio de cópias dos seguintes documentos: CNH (Carteira Nacional de Habilitação); CRLV (Certificado de Registro e Licenciamento do Veículo); Comprovante de seguro (se aplicável). A participação nesta etapa é obrigatória para a continuidade no processo. A IQVIA está empenhada em adotar um ambiente de trabalho diverso e inclusivo. Nosso objetivo é atrair e reter as melhores pessoas, independentemente de gênero, raça, estado civil, origem étnica, nacionalidade, idade, deficiência, orientação sexual, identidade de gênero ou qualquer outra característica. Junte-se a nós! ⚠️A IQVIA realiza contato com candidatos exclusivamente por meio de seus canais oficiais de recrutamento, incluindo e-mails corporativos com domínio @iqvia.com e plataformas de seleção autorizadas pela empresa. Caso receba uma comunicação suspeita em nome da IQVIA por canais não oficiais, recomendamos que não compartilhe informações pessoais e entre em contato conosco pelos canais oficiais para verificação. #LI-CES#LI-DNP#LI-LATAM IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

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    Vaga PCD Assistente Administrativo de Pesquisa Clínica - Exclusivo para Pessoas com Deficiência (Pessoa Com Deficiência - PCD)

    IQVIA
    São Paulo - SP

    Somente PCD - This is a talent pool for people with disabilities. If you do not belong to this group and wish to apply, you can apply for other vacancies within IQVIA jobs. Job OverviewPerform daily administrative activities, in conjunction with the Clinical Research Associates and Regulatory and Start-Up teams, to ensure a complete and accurate Trial Master File delivery. Essential Functions• Assist Clinical Research Associates (CRAs) and Regulatory and Start-Up (RSU) team with accurately updating and maintaining clinical documents and systems (e.g., Trial Master File (TMF)) that track site compliance and performance within project timelines.• Assist the clinical team with the preparation, handling, distribution, filing, and archiving of clinical documentation and reports according to the scope of work and standard operating procedures.• Assist with periodic review of study files for completeness.• Assist CRAs and RSU with preparation, handling and distribution of Clinical Trial Supplies and maintenance of tracking information.• Assist with the tracking and management of Case Report Forms (CRFs), queries and clinical data flow.• Act as a central contact for the clinical team for designated project communications, correspondence and associated documentation. Qualifications• Bachelor's Degree Life sciences ideally, but not mandatory.• Ideally 1 years’ experience in a healthcare environment or equivalent combination of education, training and experience. Other administrative experience is highly valuated.• Upper-intermediate level of English. • Excel knowledge is highly appreciated. • Hybrid role: offices are in Sao Paulo, SP. Please, submit your CV and laudo when applying. #LI-NRJ #LI-Hybrid IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

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    Vaga PCD Pharmacovigilance Specialist (Fluent in English + German) (Pessoa Com Deficiência - PCD)

    IQVIA
    São Paulo - SP

    Somente PCD - Job Overview Review, assess, and process safety data and information across service lines, received from various sources. Distribute reports/data to both internal and external third parties following applicable regulations, Standard Operating Procedures (SOPs), and internal guidelines under the guidance and support of senior operation team members. This is a trilingual role requiring fluency in English, Spanish, and German. Main Responsibilities Process safety data according to applicable regulations, guidelines, SOPs, and project requirements.Perform pharmacovigilance activities, including collecting and tracking incoming Adverse Events (AEs) and endpoint information, determining initial/update status of incoming events, database entry, coding AEs and products, writing narratives, and literature-related activities.Ensure compliance with quality, productivity, and delivery standards per project requirements.Liaise with different functional team members and healthcare professionals to address project-related issues. Qualifications Bachelor’s degree in Life sciences or a related field (mandatory)Fluency in English and German (mandatory) (will be evaluated)Up to 3 years of previous clinical experience (desirable)1 year of pharmacovigilance experience will be highly valued (desirable) IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

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    Vaga PCD Clinical Scientist, Clinical Science, Cronos (Pessoa Com Deficiência - PCD)

    IQVIA
    São Paulo - SP

    Somente PCD - IQVIA provides scientific services spanning clinical trials, real world evidence, and consulting in all areas of the product lifecycle. The Patient Centered Solutions (PCS) team leads the industry in generating data to ensure that the patient voice is incorporated into the development and commercialization of medication and other drug/non-drug interventions. We focus on understanding and meeting the needs of our clients – mostly life science/pharmaceutical companies – through the application of broad consulting expertise and technical scientific knowledge to design scientifically rigorous research. This research is broad and includes qualitative (e.g. interviews, focus groups), quantitative (e.g. clinical outcome assessments (COAs)/patient-reported outcomes (PROS), preference research) and passive (e.g. digital health technology tools) approaches to understand patient, caregiver and healthcare professional experiences and expectations of disease and treatment. To meet our client expectations and retain the excellent reputation built up over time the IQVIA PCS team is committed to recruiting, training and supporting driven individuals who have both consulting skills and life science skills that can be applied to PCS research activities. Individuals joining us are assured of a rewarding and progressive career in patient-focused research. You’ll have the opportunity to address challenging client issues, across multiple geographies with a hands-on influence in developing and delivering solutions. We operate in a truly multi-cultural, collegial and collaborative work environment that is rich in development and growth. Role & Responsibilities The role-holder will need to be a committed individual, who combines high emotional intelligence and excellent communication skills. They will thrive in a fast-paced environment and be comfortable managing conflicting priorities. The environment is dynamic and ever-changing, moving at the pace of our clients’ needs and the candidate will be expected to understand the sense of urgency that is synonymous with the business. As a Consultant, ClinRO Services within the PCS team at IQVIA, you will directly administer assessments to participants in a clinical trial, or evaluate the quality of assessments performed by others and provide feedback regarding interview technique and scoring. Responsibilities include: Review of scales administered by raters in a clinical trial to ensure that assessments are being conducted in a standardized manner to ensure data reliability. Evaluation the quality of assessments, conducting live interactions with raters to discuss assessment methodology, scoring technique, and to provide guidance, as necessary. Evaluate case data and appropriately prepare for discussions with raters (e.g., prepared to discuss relevant issues and scale items, and have necessary documents available). Complete rater interactions and assigned tasks as scheduled. Responsible for timely submission of all documentation associated with assigned tasks. Participate in all orientation, training and calibration activities as required. Functional assessments of rater performance (e.g., mock interview) and assistance in preparing and disseminating communications. Contacting clinical trial participants remotely (e.g., via proprietary app, Engage) to administer assessments, and will appropriately document resultant information (e.g., notes, scores) What do you need to apply? Minimum of a Master’s degree (MA/MS) in Psychology, Counseling, Psychiatric, Nursing or Social Work, or equivalent. Minimum of 3 years’ clinical experience working with schizophrenia and major depressive disorder populations. Minimum of 3 years clinical experience working administering psychiatric assessments including the PANSS, to these populations is also required. Clinical Trials experience preferred. Advanced level of English. Home based position in Latin America. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

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    Vaga PCD SES Project Lead (Pessoa Com Deficiência - PCD)

    IQVIA
    São Paulo - SP

    Somente PCD - Role Overview: The Site Enablement Solutions team at IQVIA provides qualified, clinically experienced research staff to clinical trial sites globally to accelerate and optimize the performance of clinical trials. By supplying sites with support for data entry, patient recruitment, patient visits, assessments, and other tasks, IQVIA is able to relieve the burden on trial sites and support our sponsors in completing their trials on time, and within budget. The goal of the Site Enablement Solutions Project Lead (SES PL) role is to optimize overall delivery of Site Enablement Solutions throughout the lifecycle of projects. The SES PL will also serve as internal consultants to the IQVIA study team and/or sponsor, present progress, and updates to sponsor, and manage overall delivery of our services on a project, including managing the Site Enablement project budget. Key Responsibilities Collaborate with pre- and post-award stakeholders to manage the coordination, planning, and implementation of Site Enablement Solutions.Develop global Site Enablement Solutions delivery strategy in identifying sites, executing on agreed upon scope and extending/expanding our services as warranted. Determine internal team resourcing based on study needs.Develop and execute operational plans on larger, multi- region studies or programs, including develop and implement risk management plans for minimizing impact on project objectives and deliverables. Establish study specific expectations and timelines.Communicate with sponsors and project teams to implement and monitor impact of Site Enablement Solutions.Provide ongoing proactive operational and tactical recommendations as needed based on study performance.Collaborate with internal and external teams to deliver site adoption and quality resource placement within specified timelines.Establish a collaborative approach for project delivery with Patient and Site Centric Solutions teams, including patient recruitment team and Direct to Patient Campaign. Schedule and facilitate internal study meetings.Represent Site Enablement Solutions at site/sponsor-facing meetings (i.e. KOM, IM, F2F/LL, etc.) to present strategy/rationale, and training.Ownership for study KPI and financial performance. Manage the scope of work, objectives, quality of deliverables, and other activities of assigned projects.Manage and oversee internal workflow management systems to ensure compliance.Other duties as assigned by management. Qualifications: Bachelors degree in life sciences or related field.Experience requires 3 - 5 years of prior relevant experience:5 years’ clinical trial experience3 years’ experience at a CRO or clinical trial services provider3 years in a Project Manager roleAdvanced level of English, you'll work with global projects and global teams. #LI-NRJ #LI-Remote IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

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    Vaga PCD Central Monitor in LATAM (Pessoa Com Deficiência - PCD)

    IQVIA
    São Paulo - SP

    Somente PCD - Job Overview A Central Monitor is a key skilled and clinically experienced team member of IQVIA Central Monitoring Department. Provides remote project support and assistance across multiple projects, sites and teams and reviews the structured clinical data output with access to medical charts. Essential Functions: Perform centralized monitoring activities on assigned projects and evaluate the quality and integrity of the study as per the protocol, SOPs, respective regulations and guideline. Ensure accurate completion and maintenance of internal systems, databases, tracking tools/reports for the project specific information. Perform Management of triggers and preparation of i-site pack for respective sites and countries for assigned study(ies). May assist in developing required basic data analytics scope and performing the trend analytics for their respective study(ies). Participate on study team meetings and interact with cross functional staff to verify information and/or triage new data issues or prior identified action items. Escalate quality issues pertaining to site to respective Centralized Monitoring Lead/ Sr. Central Monitor. May perform Subject Level Data Review that require further investigation with the clinical site to determine overall accuracy (inclusion & exclusion criteria/ IP/AE/ Labs/EOT/EOS/ End points/SAEs etc.) Review any other information as necessary to determine overall readiness of the patient information for next level review. Interaction with sites/CRA and follow-up on study required milestones from the project start until close out. May act as backup/ perform the activities as per the task list delegated by Central Monitor Expert/Centralized Monitoring Lead. Qualifications: Bachelor's degree in life sciences or related field, or nursing qualification; or be near to obtain the degree - Mandatory. +2 years of monitoring experience (on site or remote) - Mandatory. Advanced level of Excel. We are looking for someone with advanced level of English - Mandatory. You could support sites either in Latin America or North America. This is a home based position. #LI-Remote #LI-NRJ IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

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    Vaga PCD CRA 2 (Pessoa Com Deficiência - PCD)

    IQVIA
    São Paulo - SP

    Somente PCD - Location: Brazil (Sao Paulo) About Us: Join our team and help shape the future of our organization. We are a leading company committed to excellence and innovation, seeking a talented Senior Recruiter to support our growth. Job Overview: Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements. Key Responsibilities: Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines. Work with sites to adapt, drive and track subject recruitment plan in line with project needs to enhance predictability. Administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issues. Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations. Escalate quality issues as appropriate. Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (CRF) completion and submission, and data query generation and resolution. May support start-up phase. Ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) verify that the Investigator's Site File (ISF) is maintained in accordance with GCP / ICH and local regulatory requirements. Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters and other required study documentation. Collaborate and liaise with study team members for project execution support as appropriate. Basic Qualifications: Bachelor's Degree Degree in scientific discipline or health care preferred. Excellent command of English (written/spoken). Basic knowledge of, and skill in applying, applicable clinical research regulatory requirements (i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines). Good therapeutic and protocol knowledge as provided in company training. Others requirements: Strong attention to detail and excellent communication skills. Exceptional problem-solving, judgment, and decision-making abilities. Computer skills including proficiency in use of Microsoft Word, Excel and PowerPoint and use of a laptop computer and iPhone and iPad (where applicable). Written and verbal communication skills including good command of English language. Organizational and problem-solving skills. Effective time and financial management skills. Ability to establish and maintain effective working relationships with coworkers, managers, and clients. Why Join Us? Be part of an innovative and forward-thinking company that collaborates to make a healthier world. Work alongside a diverse and talented team. Many opportunities for professional growth by developing project mgmt abilities. Competitive salary and benefits package. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

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    Vaga PCD Sr. Site Activation Specialist (North America team) (Pessoa Com Deficiência - PCD)

    IQVIA
    São Paulo - SP

    Somente PCD - Job OverviewPerform tasks at a country level associated with Site Activation (SA) activities in accordance with applicable local and/or international regulations, standard operating procedures (SOPs), project requirements and contractual/budgetary guidelines. May also include maintenance activities. Developing professional individual contributor who works under moderate oversight and supervision. Responsible for making recommendations for enhancements in systems and processes to solve problems or improve effectiveness of job area. Problems faced are general and may require understanding of broader set of issues but are not complex.Essential Functions• Under general supervision, serve as Single Point of Contact (SPOC) in assigned studies for investigative sites, Site Activation Manager (SAM), Project Management team, and other departments as necessary. Ensure adherence to standard operating procedures (SOPs), Work Instructions (WIs), quality of designated deliverables and project timelines.• Perform feasibility, site ID, start up and site activation activities according to applicable regulations, SOPs and work instructions. Distribute completed documents to sites and internal project team members.• Prepare site documents, reviewing for completeness and accuracy.• Ensure accurate completion and maintenance of internal systems, databases and tracking tools with project specific information.• Review and provide feedback to management on site performance metrics.• Review, establish and agree on project planning and project timelines. Ensure monitoring measures are in place and implement contingency plan as needed.• Inform team members of completion of fesibility, site ID, regulatory and contractual documents for individual sites.• Review, track and follow up the progress, the approval and execution of documents, questionnaires, CDA/SIF, regulatory, ethics, Informed Consent Form (ICF), and Investigator Pack (IP) release documents, in line with project timelines.• Provide local expertise to SAMs and project team during initial and on-going project timeline planning.• Perform quality control of documents provided by sites.• May have direct contact with sponsors on specific initiatives.Qualifications• Based in Argentina or Brazil.• Bachelor's Degree Life science or related field mandatory.• 3 years clinical research experience supporting site activation/regulatory tasks.• Advanced level of English is mandatory. You will be working with a global team, and supporting North American sites. Please, make sure to submit your CV in English. It will be assessed by a global team. ⚠️ IQVIA contacts candidates exclusively through its official recruitment channels, including corporate email addresses ending in @iqvia.com and company-authorized recruitment platforms.If you receive a suspicious communication claiming to be from IQVIA through unofficial channels, we recommend that you do not share any personal information and contact us through our official channels for verification. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

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    Vaga PCD Senior Medical Data and Safety Review Physician (Pessoa Com Deficiência - PCD)

    IQVIA
    São Paulo - SP

    Somente PCD - JOB SUMMARY: Responsible for medical data review and medical safety case processing and related safety activities. Performs review of medical data to ensure medical/scientific plausibility and to employ medical assessment and knowledge. Also, provides medical expertise in assigned trials and standalone safety projects. Train and mentor team members in medical and safety review activities. ESSENTIAL JOB FUNCTIONS, DUTIES AND RESPONSIBILITIES: Attend and present Medical Data Review activities during the client Kick Off Meeting. Write Medical Data Review Plan in collaboration with the Medical Monitor and in accordance with the client input. Create protocol specific Medical Data Review Guide in collaboration with the Medical Monitor. Participate in the internal eCRF review meeting and contribute to the development of eCRF. Define data capture requirements as required throughout the study that are consistent with the protocol and reporting needs. Contribute to the Data Review Plan. Provide requirements and specifications for programming of data listings. Collaborate with Clinical Science and Data Operations teams in the development of Qlik Sense builds and protocol specific customizations for patient profiles. Participate in activities involving risk assessment and measuring the effectiveness of risk minimization measures. Provide medical review of data listings and patient profiles, including but not limited to, adverse events, concomitant medications, medical history, labs, vitals, ECGs, eligibility criteria, efficacy assessments and study specific assessments. Prepare protocol specific templates for the periodic summary reports for safety data, including the Safety Trend Analysis Report (STAR) or Safety Review Committee slide presentations, in collaboration with the Medical Monitor. Compose the STAR report during the study according to scope and timelines. Conduct in-stream data trend analysis in support of data quality and integrity including protocol compliance and targeted review of patient data. Prepare periodic MDR summary reports or presentations if requested. Medical review and case assessment of SAEs including assessment and coding of preferred term, medical history, indications of concomitant medications and treatment medications; determination of seriousness, causality, expectedness; narrative review; query generation and follow up of SAE till case closure. Compose sponsor comment/summary. Compose, edit, and medically review Analyses of Similar Events (AOSE) for expedited cases as appropriate based on regulatory requirements. MINIMUM REQUIRED EDUCATION AND EXPERIENCE: Medical degree from an accredited, internationally recognized medical school. Recipient of a medical license from the country or region in which he/she currently resides or previously resided. 5 years of experience in the practice of medicine in a clinical or academic setting which may include specialty medical training or fellowship. Minimum of 3 years of experience in Medical Data Review and/or Medical Safety Review. Advanced English level. Knowledge of MedRA, WhoDrug. Previous experience in Medidata Rave, Inform. Previous experience in Argus Safety. Solid experience with Excel, Power Point and other data visualization tools as Spotfire, J Review, others. Availability to work in a flexible global schedule. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

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    Vaga PCD Assoc. Central Monitor or Central Monitor (French speaker) (Pessoa Com Deficiência - PCD)

    IQVIA
    São Paulo - SP

    Somente PCD - Job Overview An Assoc Central Monitor or Central Monitor is a key skilled and clinically experienced team member of IQVIA Central Monitoring Department. Provides remote project support and assistance across multiple projects, sites and teams and reviews the structured clinical data output with access to medical charts. Essential Functions: Perform centralized monitoring activities on assigned projects and evaluate the quality and integrity of the study as per the protocol, SOPs, respective regulations and guideline. Ensure accurate completion and maintenance of internal systems, databases, tracking tools/reports for the project specific information. Perform Management of triggers and preparation of i-site pack for respective sites and countries for assigned study(ies). May assist in developing required basic data analytics scope and performing the trend analytics for their respective study(ies). Participate on study team meetings and interact with cross functional staff to verify information and/or triage new data issues or prior identified action items. Escalate quality issues pertaining to site to respective Centralized Monitoring Lead/ Sr. Central Monitor. May perform Subject Level Data Review that require further investigation with the clinical site to determine overall accuracy (inclusion & exclusion criteria/ IP/AE/ Labs/EOT/EOS/ End points/SAEs etc.) Review any other information as necessary to determine overall readiness of the patient information for next level review. Interaction with sites/CRA and follow-up on study required milestones from the project start until close out. May act as backup/ perform the activities as per the task list delegated by Central Monitor Expert/Centralized Monitoring Lead. Qualifications: Based in Argentina, Brazil, Mexico, Peru, Colombia or Chile. Bachelor's degree in life sciences or related field, or nursing qualification; or be near to obtain the degree - Mandatory. For the Central Monitor role: +2 years of monitoring experience (on site or remote). For the Assoc. Central Monitor role: +2 years of study coordinator experience. We are looking for someone with advanced level of English & French mandatory. You will support sites in North America (US and Canada) and may support sites in Latin America. Both languages will be evaluated. Advanced level of Excel. This is a home based position. #LI-Remote #LI-NRJ ⚠️ IQVIA contacts candidates exclusively through its official recruitment channels, including corporate email addresses ending in @iqvia.com and company-authorized recruitment platforms. If you receive a suspicious communication claiming to be from IQVIA through unofficial channels, we recommend that you do not share any personal information and contact us through our official channels for verification. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

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    Vaga PCD Analyst - Global HE/HTA (Pessoa Com Deficiência - PCD)

    IQVIA
    São Paulo - SP

    Somente PCD - OVERVIEW Our industry-leading team is growing and seeking an enthusiastic technical specialist to support our Evidence Synthesis practice and Centre of Excellence (CoE). The role involves primarily the development of off-the-shelf coding scripts, efficiency and automation tools for the CoE and contribution in highly complex statistical projects that require de novo conceptualisation and out-of-the-box thinking. You can expect a blend of statistical/ technical activities, strategic problem-solving for complex research tasks, coding/programming, enhancing existing and developing new capabilities. RESPONSIBILITIES Support the development of internal tools and software to drive automation efficiency and methods development in evidence synthesis for HTA. Develop technical guidance for associated tools Edit, review, and develop scripts to ensure accurate and efficient implementation tailored to specific research problems. Proficiency and demonstrable coding/programming experience in R is required, and knowledge of Stan is desirable as well as WinBUGS, OpenBUGS, JAGS. Establish research credentials and further the wider IQVIA profile in evidence synthesis through the development of innovative methods and the dissemination of research outputs in peer-reviewed journals and scientific conferences Be an active member of the Centre of Excellence for Evidence Synthesis and develop core material to increase automation and efficiency across IQVIA For a small proportion of time, support project implementation primarily on complex projects that require de novo material development and out-of-the-box thinking QUALIFICATIONS, EXPERIENCE, TECHNICAL AND PERSONAL SKILLS Masters (required) or PhD (plus) in statistics, biostatistics, mathematics, health economics or a related discipline. Fluency in English (spoken and written - this role is part of a global team) Relevant experience working as a statistician or evidence synthesis specialist in academia or consultancy, CRO, pharmaceutical/biotech or academia (as post-graduate researcher) Strong programming skills in R, ability to provide evidence of this applied in a business or academic setting Experience in software development ideally on RShiny applications. Excitements and willingness to improve and software development skills Excellent analytical and problem-solving skills, including in the context of client strategic challenges Excellent scientific writing skills, oral communication, ability to convey technically complex issues to non-technical audiences and teams, attention to detail Efficient time- and project-management, proactive communication, team spirit Good understanding of related HEOR domains and Evidence Synthesis processes *Resume/CV must be submitted in English* #home-based #remote A IQVIA está empenhada em adotar um ambiente de trabalho diverso e inclusivo. Nosso objetivo é atrair e reter as melhores pessoas, independentemente de gênero, raça, estado civil, origem étnica, nacionalidade, idade, deficiência, orientação sexual, identidade de gênero ou qualquer outra característica. Junte-se a nós! IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

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    Vaga PCD Legal Specialist 1 (Contracts) (Pessoa Com Deficiência - PCD)

    IQVIA
    São Paulo - SP

    Somente PCD - AREA OVERVIEW:This position forms part of the Lead Contract Negotiators (LCN) group which supports the organization’s clinical agreements globally. Provides legal advice and counsel within a function, region or country to support the creation, review and negotiation of and non-disclosure and vendor agreements, and supports contracting process from triage to contract metric reports. RESPONSAIBILITIES: Reviewing, drafting and negotiating a broad range of clinical contracts (i.e. primarly non-disclosure agreements, vendor agreements and other customer agreements as needed). Ensuring that contracts are in compliance with legal, regulatory and organization policies. Monitoring the contract process to assure compliance with the organization’s contractual guidelines for both customers and vendors, including participation in precontract discussions, contract negotiations and contract changes. Track work and obtain appropriate reviews and approvals, adhering to established processes. Participate or coordinate as a legal contract lead in customer or vendor calls to support negotiations of the contracts. Ensure delivery of a final contract in a timely fashion, working independently or as part of a team. Conduct written and/or verbal follow-up with customers and vendors after the delivery of draft or signature-ready contracts. Support LCN triage activities, track team workload and contract metrics. REQUIRED KNOWLEDGE, SKILLS AND EXPERIENCE: Bachelor Law Degree completed + local bar association active. Qualified to practice law in a global organization and relevant experience related to contracts. Advanced/fluent English skills (this role is part of a Global team) Proficient in drafting various type of contracts in English and negotiating complex deals directly with customers and vendors. Strong organizational, planning, project and contract management, communication, presentation and influence skills. Ability to work creatively in a fast-paced environment Exceptional attention to detail and ability to work simultaneously on multiple priorities and meet stablished timelines Possess excellent interpersonal and relationship building skills necessary to establish quickly credibility and trust throughout the organization. Excellent skills using MS Office Suite: MS Word, MS PowerPoint and MS Excel. Prior in-house experience in the pharmaceutical industry and/or familiarity with drug discovery and development process will be a plus. *Resume/CV must be submitted in English* #home-based #remote IQVIA is committed to embracing a diverse and inclusive work environment. Our goal is to attract and retain the best people, regardless of their gender, race, marital status, ethnic origin, national origin, age, disability, sexual orientation, gender identity or any other characteristic. Join us! ⚠️ IQVIA contacts candidates exclusively through its official recruitment channels, including corporate email addresses ending in @iqvia.com and company-authorized recruitment platforms. If you receive a suspicious communication claiming to be from IQVIA through unofficial channels, we recommend that you do not share any personal information and contact us through our official channels for verification. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

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    Vaga PCD Estagiário de Client Services (Pessoa Com Deficiência - PCD)

    IQVIA
    São Paulo - SP

    Somente PCD - Sobre a IQVIA: A IQVIA é líder global em Human Data Science, oferecendo soluções integradas de pesquisa clínica, informação e tecnologia para o setor de saúde. Combinando dados, expertise analítica e inovação, apoiamos nossos clientes na melhoria de seus resultados clínicos, científicos e comerciais. Sobre a oportunidade: Estamos em busca de um estagiário para atuar na área de Atendimento ao Cliente, apoiando a gestão de demandas, relacionamento com clientes e acompanhamento de entregas. Principais responsabilidades: Apoiar o atendimento e o relacionamento com clientes da carteira, prestando suporte de primeiro nível para dúvidas e solicitações relacionadas às soluções IQVIA; Acompanhar demandas e prazos junto às áreas internas, garantindo o correto direcionamento e a resolução dos chamados; Atuar na resolução de solicitações e dúvidas dos clientes em conjunto com o time; Organizar informações, relatórios e apoiar nas rotinas administrativas da área de Atendimento ao Cliente; Acompanhar o status das solicitações e manter os clientes atualizados sobre o andamento dos casos; Realizar análises básicas de dados e informações de mercado; Dar suporte no controle de entregas e na qualidade dos serviços prestados; Apoiar o coordenador e os analistas na gestão das contas da equipe; Participar de reuniões com clientes, contribuindo para o acompanhamento e entendimento das demandas. Requisitos: Cursando ensino superior (Administração, Marketing, Comunicação, Engenharia ou áreas correlatas) Boa comunicação e organização Perfil analítico e proatividade Conhecimento básico em Excel/PowerPoint Inglês será considerado um diferencial Disponibilidade de 2 anos para estagiar O que oferecemos: Ambiente colaborativo e de aprendizado contínuo Oportunidade de desenvolvimento em uma empresa Global Exposição a projetos relevantes e contato com clientes estratégicos Local de Trabalho: Escritório da IQVIA localizado na Chácara Santo Antônio (São Paulo), próximo à estação Granja Julieta (Atuação híbrida de 4x presencial). A IQVIA está empenhada em adotar um ambiente de trabalho diverso e inclusivo. Nosso objetivo é atrair e reter as melhores pessoas, independentemente de gênero, raça, estado civil, origem étnica, nacionalidade, idade, deficiência, orientação sexual, identidade de gênero ou qualquer outra característica. Junte-se a nós! ⚠️A IQVIA realiza contato com candidatos exclusivamente por meio de seus canais oficiais de recrutamento, incluindo e-mails corporativos com domínio @iqvia.com e plataformas de seleção autorizadas pela empresa. Caso receba uma comunicação suspeita em nome da IQVIA por canais não oficiais, recomendamos que não compartilhe informações pessoais e entre em contato conosco pelos canais oficiais para verificação. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

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    Vaga PCD CRA 1 (Pessoa Com Deficiência - PCD)

    IQVIA
    São Paulo - SP

    Somente PCD - Location: Brazil (Sao Paulo) About Us: Join our team and help shape the future of our organization. We are a leading company committed to excellence and innovation, seeking a talented Senior Recruiter to support our growth. Job Overview: Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements. Key Responsibilities: Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines. Work with sites to adapt, drive and track subject recruitment plan in line with project needs to enhance predictability. Administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issues. Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations. Escalate quality issues as appropriate. Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (CRF) completion and submission, and data query generation and resolution. May support start-up phase. Ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) verify that the Investigator's Site File (ISF) is maintained in accordance with GCP / ICH and local regulatory requirements. Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters and other required study documentation. Collaborate and liaise with study team members for project execution support as appropriate. Basic Qualifications: Bachelor's Degree Degree in scientific discipline or health care preferred. Excellent command of English (written/spoken). Basic knowledge of, and skill in applying, applicable clinical research regulatory requirements (i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines). Good therapeutic and protocol knowledge as provided in company training. Others requirements: Strong attention to detail and excellent communication skills. Exceptional problem-solving, judgment, and decision-making abilities. Computer skills including proficiency in use of Microsoft Word, Excel and PowerPoint and use of a laptop computer and iPhone and iPad (where applicable). Written and verbal communication skills including good command of English language. Organizational and problem-solving skills. Effective time and financial management skills. Ability to establish and maintain effective working relationships with coworkers, managers, and clients. Why Join Us? Be part of an innovative and forward-thinking company that collaborates to make a healthier world. Work alongside a diverse and talented team. Many opportunities for professional growth by developing project mgmt abilities. Competitive salary and benefits package. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

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    Vaga PCD Sr Sourcing Recruiter (Pessoa Com Deficiência - PCD)

    IQVIA
    São Paulo - SP

    Somente PCD - Job OverviewAs a Sr Sourcing Recruiter in Talent Search at IQVIA, you will play a pivotal role in shaping our talent acquisition strategy by partnering closely with recruiters, hiring managers, and business leaders. This role is ideal for a proactive, data-driven, and collaborative professional who thrives in a fast-paced environment and is passionate about identifying top talent to drive business success. Key ResponsibilitiesStrategic Partnership: Collaborate with recruiters and hiring managers across designated departments to understand hiring needs and develop tailored sourcing strategies.Intake Leadership: Lead intake meetings to define role requirements, set expectations, and align on recruitment timelines and goals.Sourcing Strategy Development: Design and execute innovative, cost-effective recruiting plans to attract high-quality candidates.Job Posting Management: Create, publish, and optimize job postings to maximize visibility and attract diverse talent.Candidate Engagement: Leverage platforms such as LinkedIn, job boards, and CRM tools to identify and engage passive candidates, promoting IQVIA’s mission and opportunities.Screening and Evaluation: Review applications, conduct initial interviews, and assess candidates’ qualifications, experience, and alignment with role expectations.Diversity and Compliance: Champion diversity hiring initiatives and ensure adherence to local and regional compliance standards.Market Intelligence: Monitor industry trends and talent market dynamics to inform sourcing strategies and hiring decisions.Data Management: Maintain accurate and up-to-date records in the ATS and CRM systems.Team Collaboration: Partner with the broader recruitment team to ensure a seamless and positive candidate experience.Analytics and Reporting: Use data and metrics to evaluate sourcing effectiveness and continuously improve recruitment strategies.Mentorship: Provide guidance and mentorship to junior Talent Search team members, fostering a culture of learning and excellence.QualificationsBachelor’s degree or equivalent combination of education, training, and experience.Proven experience in a Talent Search or Recruiter role, preferably in a fast-paced, global organization.Strong relationship-building skills with stakeholders at all levels.Demonstrated commitment to continuous learning and staying current with talent acquisition trends.Cultural awareness and sensitivity in a diverse hiring environment.Excellent organizational, time management, and communication skills.Proficiency in Boolean search techniques and sourcing tools.Strong analytical and problem-solving abilities.Adaptability and resilience in a dynamic work environment. Why IQVIA?At IQVIA, we are committed to advancing human health through data science, technology, and deep domain expertise. Join a team that is passionate about innovation, collaboration, and making a meaningful impact on global healthcare. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

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    Vaga PCD Investigator Site Payments Analyst (Pessoa Com Deficiência - PCD)

    IQVIA
    São Paulo - SP

    Somente PCD - We are looking for an enthusiastic associate interested in supporting clinical trials and payments activities with the sites, to join our FSP team. Job Overview You will provide support enabling the accurate and timely payment administration to our network of project sites. Perform duties in accordance with IQVIA Finance Standard Operating Procedures (SOPs), Sarbanes-Oxley Controls and Unit Service Level agreements (if applicable). Essential Functions • Managing a portfolio of projects and providing oversight on the entire process. Ability to form remote relationships with colleagues across the globe, consider indirect influences on your work and manage these.• Highlighting aged invoices and financial risks – give reasons why for any delays.• Data quality control, ensuring batches are scheduled as per contracts and meeting the budgets.• Project reconciliations.• Payment cycle target trending – ensuring the studies are meeting the target for each step in the payment cycle.• Providing high level of customer service to internal project teams and assisting them in any project related issues by finding resolution. Ability to influence others and ensure that key actions are taken.• Track and report metric data flagging nonstandard issues to project teams / line manager.• Provide assistance to other team members as required, to ensure the group meets targets.• Check that appropriate approvals are obtained for set up and payment process.• Provide support and participate in teams handling various routine tasks.• Provide standard reports and run KPI for the project teams.• Perform other duties as assigned.• File appropriate documents. Education and Experience Requirements • Graduated - Bachelor’s degree in appropriate scientific or business disciplines. • Excellent oral & written communication in English (advance level). • 1-3 years of experience and/or equivalent competencies in pharmaceutical industry/clinical research. • Previous experience in systems would be an advantage however full training will be provided. • Ability to work effectively in cross functional teams. • Strong and proven analytical and problem resolution skills. • Working knowledge of PCs (MS Office suite at a minimum). • Must demonstrate innovative spirit and ability to accomplish substantial tasks with minimal supervision. • Good written and oral communication skills as appropriate. • Home based role. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

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    Vaga PCD Site Contracts Associate, Brazil, IQVIA Biotech (Pessoa Com Deficiência - PCD)

    IQVIA
    São Paulo - SP

    Somente PCD - IQVIA Biotech is hiring for Site Contracts Associate with 1-3 years' experience negotiating clinical site contracts and budget templates. IQVIA Biotech is a full-service CRO purpose-built to serve biotech sponsors. With over 25 years of experience, we offer agile, therapeutically aligned solutions and trusted partnerships that help bring breakthrough treatments to patients faster. Job Overview We are seeking a Site Contract Specialist to support the development and execution of investigator grant estimates and site contracting activities for clinical trials. This role plays a critical part in ensuring timely and compliant study start-up and maintenance by managing financial and operational aspects of site contracts. Essential Functions Develop investigator grant estimates and proposal text to support business development and proposal creation. Utilize and maintain contract and budget templates, systems, tools, and training materials for assigned sponsors, studies, or programs in alignment with the Scope of Work and Project Plan. Collaborate with sponsors, internal stakeholders, and regional/country teams to ensure successful delivery of project scope and compliance with sponsor requirements and RSU Management Plans. Provide specialized operational and financial contracting support to enable efficient trial initiation and maintenance while ensuring regulatory compliance. Assist in the creation and review of scientific, technical, and administrative documentation to support study start-up and ongoing trial activities. Contribute to the collection, analysis, and dissemination of contracting intelligence to support assigned studies and broader organizational needs. Monitor contracting efficiency and adherence to timelines and financial goals; report performance metrics and out-of-scope activities as needed. Ensure compliance with contract management and quality standards. Provide administrative and operational support to contract analysts, managers, and directors. Maintain accurate records in internal systems including CTMS, databases, tracking tools, and project plans. Qualifications Bachelor’s degree in business, life sciences, or a related field preferred. Experience in clinical trial budgeting, contracting, or site management strongly preferred. Strong understanding of clinical research processes and regulatory requirements. Proficiency in Microsoft Office and contract management systems. Excellent organizational, analytical, and communication skills. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

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    Vaga PCD Connected Devices Project Manager (Pessoa Com Deficiência - PCD)

    IQVIA
    São Paulo - SP

    Somente PCD - Job Overview Manage small to medium size Connected Devices that are stand-alone or full-service in scope, across all clinical trial phases. With support from Senior Project Manager, ensure all project work is completed to the sponsor's satisfaction, on time and within budget and in accordance with policies and procedures. Essential Functions • Under supervision, plan, initiate, execute, control, and deliver projects in accordance with the Scope of Work agreed with the customer. • Lead the Connected Devices cross-functional teams to ensure successful delivery of assigned projects. • Ensure that consistent and appropriate project specific guidelines are documented and circulated to all project team members and that the team is well-trained on these guidelines. • Track project progress, identify and evaluate project risks and take advice from superiors on corrective action as appropriate. • Prepare and present project information at internal and external meetings. • With guidance, manage the project financials accurately and appropriately ensuring project goals are achieved according to customer’s expectations and within the scope of the project. Ensure revenue recognition and forecasts are calculated accurately and change orders executed where appropriate. • Conduct an ‘End of Project’ review meeting to ensure that all project activities have been completed in full. • Keep Connected Devices leadership fully informed of any project issues that may impact quality, budget, and timeliness of project delivery to the customer’s satisfaction. Request support and advice for timely issue resolution as required. • Provide input to line managers on their project team members’ performance relative to project tasks to aid career development. Qualifications • Bachelor's Degree Life science or health care related discipline • Clinical Trial Industry experience • Three years of PM experience • Experience with Microsoft Project • Risk management skills • Equivalent combination of education, training and experience • Good leadership skills • Good ability to prioritize, schedule and organize • Good interpersonal and communication skills • Good problem-solving skills • Excellent customer service skills • Good Microsoft Office skills • Ability to establish and maintain effective working relationships with coworkers, managers and clients IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

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    Vaga PCD Commercial Business Partner (Pessoa Com Deficiência - PCD)

    IQVIA
    São Paulo - SP

    Somente PCD - Role Summary The (Associate) Commercial Business Partner supports the Commercial Business Partnering function across the Real World Evidence (RWE) portfolio. The role provides structured commercial, financial, and operational support across the end-to-end opportunity and project lifecycle, partnering with Principals In Charge (PICs) and cross-functional stakeholders to ensure accuracy, compliance, and delivery against revenue and margin objectives. Key Responsibilities Forecast revenue for assigned Offering(s) through regular monitoring of the pipeline and active opportunities, in coordination with Local and Global Sales & Delivery Teams Act as a key partner to PICs by providing end-to-end project lifecycle support, including opportunity setup guidance, execution assistance, pass-through management and invoicing Drive process consistency, governance adherence, and operational efficiency Conduct regular project profitability reviews to understand performance drivers and trends, and identify opportunities for margin improvement Provide financial and commercial analysis to support performance and decision-making Act as a key point of contact for project-level financial and operational queries across RWE stakeholders for assigned Offering(s) Support Annual Sales Incentive Plan administration and tracking Ad-hoc tasks and analyses, as required Skills, Education, Experience and Competencies Typically requires 3-5 years’ business controlling or project finance experienceUniversity degree (Master / Bachelor) in Finance, Accounting, or Business Administration or equivalentKnowledge of revenue recognition, forecasting, variance analysis, month-end processes and P&L managementStrong Excel and systems capability (CRM, SAP, Hyperion or equivalent)Experience working with commercial and financial dataHighly numerate with strong analytical skills and excellent attention to detailAbility to manage multiple stakeholders in a matrixed environment Proactive, solution-oriented mindsetStrong communication and stakeholder engagementCollaborative team playerAbility to prioritize tasks and operate in a fast-paced, evolving environmentFluency in English (spoken and written) to a strong business standard *Resume/CV must be submitted in English* IQVIA is committed to embracing a diverse and inclusive work environment. Our goal is to attract and retain the best people, regardless of their gender, race, marital status, ethnic origin, national origin, age, disability, sexual orientation, gender identity or any other characteristic. Join us! ⚠️ IQVIA contacts candidates exclusively through its official recruitment channels, including corporate email addresses ending in @iqvia.com and company-authorized recruitment platforms. If you receive a suspicious communication claiming to be from IQVIA through unofficial channels, we recommend that you do not share any personal information and contact us through our official channels for verification. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

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    Vaga PCD Associate, Project Manager (Pessoa Com Deficiência - PCD)

    IQVIA
    São Paulo - SP

    Somente PCD - Job OverviewMaintains and validates the project scope, plans and schedules for moderately complex projects; adheres to established metrics for project success; applies standards (e.g. delivery process, roles and responsibilities, operational norms, compliance) Essential Functions• Maintains and validates the project scope, plans and schedules for moderately complex projects; adheres to established metrics for project success; applies standards (e.g. delivery process, roles and responsibilities, operational norms, compliance).• Monitors identified risks to program success and informs applicable stakeholders.• Manages project delivery process, scope, and costs of non-complex projects under broad supervision; drives completion of the project.• Manages stakeholder relationships; executes technical project communication plan.• Manages change by identifying impacts of the project, building awareness and support for change within the organization.• Evaluates project results against success metrics; recommends changes to processes, resources and solutions that improve productivity and end product.• Delivers established team reporting and guidance metrics. Qualifications• Bachelor's Degree Computer Science, a related field, or equivalent experience Req• Three (3) years of experience in a systems development environment• Good technical and commercial awareness• Ability to identify and understand business needs and formulate technical proposals to meet those identified business needs.• Excellent communication skills.• Excellent conversational and business English (written and oral) C1, or C2 levels IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

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    Vaga PCD Site Activation Manager (Global) (Pessoa Com Deficiência - PCD)

    IQVIA
    São Paulo - SP

    Somente PCD - Internal Job DescriptionSite Activation Manager (Global) Sponsor Facing Homebased Job Overview Lead and manage the strategic, operational, and financial delivery of Site Activation activities across assigned studies and regions. This role is responsible for accelerating site activation to support timely patient enrollment, including Site Identification and Selection, Ethics and Regulatory submissions, and Site Contracting in line with sponsor and company requirements. Key Responsibilities Provide strategic oversight and project management for global or multi-regional Site Activation activities. Lead start-up delivery (pre-award through activation) and lifecycle maintenance in compliance with ICH-GCP, regulatory requirements, and project timelines. Develop and execute the Site Activation Management Plan aligned with study strategy and scope of work. Collaborate with internal teams, regions, and external stakeholders to ensure efficient study start-up execution. Oversee regulatory submissions, approvals, contracts, and essential document processes. Assess regulatory landscapes and contribute to regulatory intelligence and strategy. Identify risks and propose practical solutions to support study delivery and bid processes. Ensure accurate tracking, reporting, and maintenance of project systems, timelines, and documentation. Support business development, including bid defense and client engagement activities. Mentor and coach team members and contribute to continuous improvement initiatives. Build and maintain strong client relationships and support customer-facing activities. Qualifications & Experience Bachelor’s degree in Life Sciences or related field. Minimum 7 years’ experience in clinical research, including 3+ years in a leadership role. Proven international project experience across multiple regions. Strong leadership and project management skills with ability to manage multiple priorities. Demonstrated ability to deliver projects on time, within scope, and budget. Excellent communication, negotiation, and stakeholder management skills. Ability to lead through others and maintain effective cross-functional relationships. Key Competencies Strategic thinking and problem-solving Leadership and team development Regulatory and clinical trial expertise Stakeholder engagement and collaboration Quality and compliance focus IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

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    Vaga PCD Associate Consultant, Advanced Analytics (Pessoa Com Deficiência - PCD)

    IQVIA
    São Paulo - SP

    Somente PCD - This is an exciting opportunity to work as an Associate Consultant in IQVIA, one of the world's leading multi-disciplinary and cross-functional teams working with Real World patient data to help our client base answer their key business questions, make more informed decisions, and deliver results. Our team offerings leverage advanced analytics, machine learning algorithms, and technology platforms for a variety of healthcare applications including finding undiagnosed patients with rare conditions, predicting patient behavior, such as switching, and understanding a patient’s diagnosis and treatment journey through the health system. As part of this team, you will be at the forefront of evolving the team’s offerings while assuming the following responsibilities: Essential Functions Business Development Support:Research clients’ business problems and find potential solutions through our offerings, while supporting proposals and client pitches. Work closely with internal stakeholders from around the business to ensure the proposed solution is truly innovative and provides an exciting value proposition to clients.Project Support:Support the design and delivery of advanced statistical/machine learning projects such as predictive modeling, patient journeys, HCP targeting, and HCP alerts. Work closely with senior consultants and data scientists to translate the clients’ business needs into statistical methodologies and be responsible for delivering the findings in clinically and commercially meaningful interpretations. Throughout the process you will apply problem solving and critical thinking, intellectual engagement, and maturity in communication.Proactively and independently manage agreed to tasks and timelines Team Support: Support and take ownership of various internal initiatives including: project automation and standardization and team building.Support the team by helping to execute new offerings Mandatory Requirements Bachelor's degree in Life Sciences, Business, Economics, Engineering, Statistics, Mathematics, Computer Science, or related field2-4 years of professional experienceStrong analytical and problem-solving skillsAdvanced Excel and PowerPoint skillsExcellent communication and stakeholder management skillsAbility to work independently and manage multiple prioritiesExperience supporting analytics/data-driven projects Nice to Have Healthcare/Life Sciences experienceSQL and/or PythonMachine Learning or GenAI exposureExperience with patient-level healthcare data IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

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    Vaga PCD Clinical Trial Psych Rater - Portuguese Speaking Speaking (Pessoa Com Deficiência - PCD)

    IQVIA
    São Paulo - SP

    Somente PCD - Clinical Trial Psych Rater - Portuguese SpeakingLocation: Remote/VirtualHours: Estimated 10–16 hours per monthRole: Clinical Specialist About IQVIA IQVIA is a global leader in advanced analytics, technology solutions, and clinical research services, dedicated to driving healthcare forward. We partner with the world’s leading pharmaceutical, biotechnology, and medical device companies to improve patient outcomes and accelerate innovation. Our team combines deep scientific expertise with cutting-edge technology to deliver high-quality data and insights that shape the future of clinical trials. Position Overview The Clinical Specialist plays a key role in ensuring the integrity and reliability of clinical trial data. This position involves reviewing scales administered by raters to confirm standardized assessment practices. Responsibilities include evaluating assessment quality, engaging in live discussions with raters to provide guidance on methodology and scoring techniques, and supporting rater performance through functional assessments (e.g., mock interviews). Additional tasks may include assisting with communication materials and documentation. Key Responsibilities Participate in all required orientation, training, and calibration activities. Review case data and prepare for rater discussions, ensuring all relevant documents and scale items are available. Conduct live interactions with raters to provide feedback and guidance on assessment methodology and scoring. Complete assigned tasks and rater interactions according to schedule. Submit all required documentation accurately and on time. Required Qualifications Education: Master’s degree (MA/MS) in Psychology, Counseling, Psychiatric Nursing, or Social Work (or equivalent). MD, DO, or PhD preferred. Experience: Minimum 3 years administering psychiatric assessments, rating scales, and/or structured clinical interviews (specifically MINI and MADRS). Minimum 3 years of clinical experience with psychiatric populations. Minimum 3 years administering scales in clinical research trials (excluding graduate/doctoral research). Experience in CNS trials preferred. Skills: Strong interpersonal and communication skills for professional interaction at all levels. Excellent organizational skills, attention to detail, time management, and problem-solving ability. Proficiency with Windows and Microsoft Office applications. Language Requirement Current openings require fluency in English and native-level proficiency in Portuguese. #LI-DNP #LI-Remote #LI-HCPN IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

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    Vaga PCD Study Start Up Manager, IQVIA (Pessoa Com Deficiência - PCD)

    IQVIA
    São Paulo - SP

    Somente PCD - Job OverviewDirect and manage the delivery of all required site activation, maintenance and regulatory activities for selected studies or multi-protocol programs, including pre-award activities, oversight of the scope of work, budget and resources. Essential Functions• Oversee the execution of Site Activation (including pre-award/bid defense activities) and/or Maintenance for assigned projects in accordance with the agreed RSU site activation strategy, adhering to project timelines. Develop, implement and maintain the Management Plan according to the Scope of Work and Project Plan, within the agreed project strategy, resolving project related issues where required. Ensure collaboration across Regulatory & Site Activation, including communication with regions and countries, to successfully deliver the agreed project scope in compliance with the RSU Management Plan. Create and/or review technical and administrative documentation to support business development and enable study initiation and maintenance, as required. Provide specialist regulatory and technical scientific support to facilitate efficient business development, initiation and maintenance of clinical trials, whilst enabling compliance with regulatory requirements. Provide overall guidance and oversight of multi-regional and multi-protocol programs during initial start-up and maintenance phase as an integral member of the study management team. Determine regulatory strategy/expectations and parameters for submissions and all necessary authorizations• identify regulatory complexity and challenges and offer creative and practical solutions to support the bid process and subsequent execution of the site activation plan. Assess and review the regulatory landscape and contribute to the collection, interpretation, analysis and dissemination of accurate regulatory intelligence to support assigned studies and wider company, as required. Execute operational strategy/ expectations for maintenance of clinical study approvals, authorizations and review/ negotiation of contracts and essential documents. Work with Quality Management to ensure appropriate quality standards for the duration of site activation (or Maintenance, as applicable). Mentor and coach colleagues as required. Ensure accurate completion and maintenance of internal systems (with emphasis on CTMS), databases, tracking tools, timelines and project plans with project specific information. May take a lead role in developing long standing relationships with preferred IQVIA customers. Deliver presentations/training to clients, colleagues and professional bodies, as required. May be involved in activities related to monthly study budget planning and reviews. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

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    Vaga PCD Sr. CRA 3, Brazil, IQVIA Biotech (Pessoa Com Deficiência - PCD)

    IQVIA
    São Paulo - SP

    Somente PCD - IQVIA Biotech is a full-service CRO purpose-built to serve biotech sponsors. With over 25 years of experience, we offer agile, therapeutically aligned solutions and trusted partnerships that help bring breakthrough treatments to patients faster. We are seeking an experienced Senior Clinical Research Associate (Sr CRA 3) to join our Clinical Monitoring team in Brazil. In this role, you will independently manage and monitor clinical trial sites to ensure studies are conducted in compliance with study protocols, Good Clinical Practice (GCP), International Council for Harmonization (ICH) guidelines, regulatory requirements, and sponsor expectations. As a key member of the study team, you will perform site monitoring activities including site qualification, initiation, routine monitoring, and closeout visits. You will partner closely with investigative sites to support patient recruitment and retention efforts, provide protocol and study-related training, and proactively identify and resolve quality or compliance issues. The Sr CRA 3 is responsible for overseeing site performance, tracking study milestones, reviewing source documentation, managing data query resolution, ensuring regulatory and essential documents are maintained, and documenting monitoring activities through timely and accurate reports. You will collaborate with cross-functional teams to support the successful execution of clinical trials and may mentor junior CRAs through co-monitoring and training activities. Qualifications Bachelor’s degree in a scientific, healthcare, or related discipline (or equivalent combination of education and experience).Minimum of 4 years of on-site clinical monitoring experience.Strong knowledge of GCP, ICH guidelines, FDA regulations, and clinical trial processes.Experience conducting monitoring visits across multiple phases of clinical research.Excellent organizational, communication, and problem-solving skills.Ability to effectively manage multiple priorities in a fast-paced environment.Proficiency with Microsoft Office applications and clinical trial systems.Preferred Skills Strong therapeutic area knowledge and protocol management experience.Proven ability to build productive relationships with investigative sites, sponsors, and internal study teams.Experience mentoring or supporting the development of junior clinical research professionals. Join us in helping accelerate the development of innovative therapies that improve patient lives worldwide. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

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    Vaga PCD Contract Negotiation Specialist (North America team) (Pessoa Com Deficiência - PCD)

    IQVIA
    São Paulo - SP

    Somente PCD - Job OverviewUnder general supervision, perform tasks at a country level associated with site activation activities in accordance with applicable local and/or international regulations, standard operating procedures (SOPs), project requirements and contractual/budgetary guidelines. The Contract Specialist is responsible for independently managing the preparation, review, and negotiation of clinical site agreements in support of study start-up activities. This role contributes directly to achieving study timelines by ensuring efficient contract execution while maintaining compliance with applicable regulations, sponsor requirements, and internal policies. Essential Functions Independently draft, review, and negotiate standard clinical trial agreements (e.g., CTAs, CDAs, amendments) with investigative sites and institutions. Manage assigned contract portfolio to support site activation deliverables and study timelines. Act as a primary point of contact for sites and internal teams for contract-related matters, ensuring clear and timely communication. Apply approved negotiation parameters and escalate non-standard terms or higher-risk issues to senior team members or Legal as needed. Collaborate with cross-functional stakeholders (e.g., Site Activation, Clinical Operations, Finance) to align contract terms, including budget-related provisions. Track contract progress and maintain accurate, up-to-date documentation in relevant systems and tools. Identify and proactively address contract-related delays, working to resolve issues and minimize impact on study timelines. Ensure all contracts comply with applicable regulatory requirements, sponsor guidelines, and company policies. Support audit and inspection readiness by maintaining complete and accurate contract files. Contribute to continuous process improvements aimed at enhancing contract cycle times and quality. Manage multiple priorities simultaneously while meeting established timelines and quality expectations. Provide regular status updates and metrics to stakeholders and project teams. Qualifications• Bachelor's degree.• At least 2 years of experience in clinical research (CRO or pharma) supporting the contract and budget negotiation with sites: direct contract/BGT negotiation experience. • Advanced level of English skills, you will be working in a team that will support sites in North America. Home based role! IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

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    Vaga PCD Sr Clinical Trial Manager - Global Studies (Pessoa Com Deficiência - PCD)

    IQVIA
    São Paulo - SP

    Somente PCD - The Sr Clinical Project Manager provide management of a clinical trial (s) in a global level. Services/deliverables include operational oversight of assigned project(s) at the global level for end-to-end project management from start-up through to closeout activities. Tasks & Responsibilities: • Ensure clinical delivery of assigned projects in compliance with regulatory requirements (International Conference on Harmonization (ICH)-Good Clinical Practice (GCP), protocol), customer requirements (contract), and internal requirements (policies, Standard Operating Procedures (SOPs), project plans).• Accountable for meeting projects’ recruitment targets and ensuring appropriate recruitment strategies are in place.• Contribute to the development of the project risk mitigation plan and manage clinical risks throughout the project’s lifecycle.• Ensure clinical quality delivery by identifying quality standards/requirements, planning how compliance will be measured, monitoring and overseeing management of clinical quality issues. Essentials Requirements: • Bachelor's Degree Health care or other scientific discipline Req• Requires 8 years clinical research/monitoring experience or equivalent combination of education, training and experience. • Minumun 3 years of regional/global trial management experience in the pharmaceutical industry or CRO.• Requires in-depth knowledge of Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines. • Nice to have Cell Therapy/Hemayology TA experience.• Requires good knowledge of project finances.• Knowledge of clinical trials - Knowledge of clinical trial conduct, and skill in applying applicable clinical research regulatory requirements i.e. International Conference on Harmonization (ICH) and Good Clinical Practice (GCP) and relevant local laws, regulations and guidelines, towards clinical trial conduct. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

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    Vaga PCD Sr. Site Activation Coordinator (North America team) (Pessoa Com Deficiência - PCD)

    IQVIA
    São Paulo - SP

    Somente PCD - Job OverviewUnder general supervision, perform tasks at a country/region level associated with site activation activities in accordance with applicable local and/or international regulations, standard operating procedures (SOPs), project requirements and contractual/budgetary guidelines. May also include feasibility or maintenance activities. Essential Functions• Under general supervision, perform feasibility, site activation and some maintenance activities in assigned studies for investigative sites, according to applicable regulations, SOPs and work instructions, working closely with the Site Activation Manager (SAM), Project Management team, and other departments as necessary. Review documents for completeness, consistency and accuracy, under guidance of senior staff.• Prepare site documents, reviewing for completeness and accuracy.• Inform team members of completion of regulatory contractual. and other documents for individual sites.• Distribute completed documents to sites and internal project team members.• Support the updating and maintenance of internal systems, databases, tracking tools, timelines and project plans with accurate and complete project specific information.• Review, track and follow up the progress, the approval and execution of required documents such as questionaires, CDAs, regulatory, ethics, Informed Consent Form (ICF) and Investigator Pack (IP) release documents. Qualifications• Bachelor's Degree Life science or related field.• With 2 years’ experience in a CRO or over 4 years of experience in a site, with previous experience in regulatory/site activation tasks. • Advanced level of English is mandatory, you'll be in touch with sites from North America. Please, submit your CV in English, it will be reviewed by a global team. This is a home based role! IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

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    Vaga PCD Consultor de Diagnóstico (Pessoa Com Deficiência - PCD)

    IQVIA
    São Paulo - SP

    Somente PCD - Visão de Trabalho Buscamos um profissional com perfil consultivo, analítico e com forte habilidade em educação médica, para atuar na gestão de contas hospitalares, especialmente voltadas à pneumologia. Essa posição exige capacidade de construir relacionamentos estratégicos com médicos e instituições, promovendo ações educacionais e facilitando o acesso ao diagnóstico e tratamento de doenças. Responsabilidades Gerenciar contas hospitalares com foco em pneumologia e especialidades correlatas;Mapear contas e estimar o potencial de atuação em cada instituição;Construir mapas de influência e fluxos internos para facilitar a jornada do paciente;Conduzir treinamentos médicos, promovendo mudança de comportamento clínico em relação à doença.Organizar e liderar eventos educacionais e reuniões clínicas;Gerar suspeitas clínicas, facilitar pedidos de testes e apoiar encaminhamentos para centros de referência;Registrar informações clínicas e operacionais com precisão, utilizando ferramentas de CRM.Requisitos Formação superior na área da saúde (Enfermagem, Farmácia, Biomedicina ou áreas afins);Experiência comprovada em gestão de contas hospitalares;Vivência com CRM e processos organizacionais;Excelente comunicação verbal e escrita;Perfil dinâmico, organizado e com empatia no trato com profissionais de saúde;Disponibilidade para viagens frequentes.CNH categoria B válidaVeículo próprio em boas condiçõesSeguro vigente.Importante: Esta posição envolve atividades externas que requerem deslocamentos frequentes para atendimento a clientes e visitas técnicas. Por isso, é indispensável que o(a) candidato(a) possua veículo próprio, Carteira Nacional de Habilitação (CNH) válida e documentação do veículo regularizada. Na etapa final do processo seletivo, será realizada a validação documental, com a solicitação do envio das seguintes cópias: CNH (Carteira Nacional de Habilitação);CRLV (Certificado de Registro e Licenciamento do Veículo);Comprovante de seguro. A participação nesta etapa é obrigatória para a continuidade no processo. A IQVIA está empenhada em adotar um ambiente de trabalho diverso e inclusivo. Nosso objetivo é atrair e reter as melhores pessoas, independentemente de gênero, raça, estado civil, origem étnica, nacionalidade, idade, deficiência, orientação sexual, identidade de gênero ou qualquer outra característica. Junte-se a nós! #LI-CES #LI-DNP #LI-LATAM IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

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    CLT

    Vaga PCD Clinical Lead - Global Study Leadership (Pessoa Com Deficiência - PCD)

    IQVIA
    São Paulo - SP

    Somente PCD - Clinical Lead (Clinical Trial Management) - Global Study Leadership At IQVIA, our Clinical Leads play a vital role in bringing innovative medicines to patients worldwide. You'll provide clinical leadership across regional and global clinical trials, partnering with Project Leaders, sponsors and cross-functional teams to ensure studies are delivered with a focus on quality, patient recruitment, site performance and operational excellence. Why Join Global Study Leadership? Global Study Leadership is a global, full-service team delivering clinical trials through both therapeutically aligned and customer-dedicated delivery models. You'll work across a diverse portfolio including Oncology, Rare Disease, CNS, Cardiovascular, Immunology, Respiratory, Cell & Gene Therapy, Infectious Disease, Ophthalmology and Women's Health while partnering with leading pharmaceutical and biotechnology sponsors around the world. Working alongside experienced project leaders and clinical operations experts, you'll have the opportunity to broaden your therapeutic expertise, strengthen your leadership capabilities and influence the successful delivery of studies that help bring new treatments to patients faster. What You'll Be Doing As a Clinical Lead, you'll be accountable for the clinical delivery of assigned studies, ensuring recruitment, site performance, quality and operational objectives are achieved while maintaining compliance with regulatory requirements and customer expectations. Key Responsibilities Lead the clinical delivery of regional and global clinical studies, ensuring projects meet quality, timeline, recruitment and operational objectivesDrive patient recruitment and site engagement strategies, ensuring enrolment targets are achieved and studies remain on trackPartner with Project Leaders and cross-functional teams to drive study milestones, resolve issues and maintain operational excellenceProvide leadership and guidance to clinical teams, supporting resource planning, training and project deliveryManage clinical risks, oversee quality standards and drive proactive mitigation strategies throughout the study lifecycleBuild strong relationships with internal and external stakeholders, ensuring effective communication and alignment across study teamsSupport financial oversight of clinical delivery, including forecasting, budget management and identification of scope changes where applicableContribute to continuous improvement initiatives, knowledge sharing and the development of less experienced team membersSupport proposal development, bid defence activities and clinical delivery planning for new opportunities where appropriate What We're Looking For Bachelor's degree in Life Sciences, Healthcare, or a related scientific discipline5+ years of clinical research, monitoring, or clinical operations experience within a CRO, pharmaceutical, or biotechnology environmentStrong understanding of clinical trial conduct, ICH-GCP guidelines and applicable regulatory requirementsExperience leading clinical study delivery activities, including patient recruitment, site management and clinical quality oversightProven ability to collaborate across cross-functional teams and manage internal and external stakeholders in a global environmentStrong communication, problem-solving, organizational and decision-making skillsExperience supporting project financial management and operational planning is desirablePassion for advancing clinical research and improving outcomes for patients worldwide IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

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    CLT

    Vaga PCD TMF Quality Project Manager (Pessoa Com Deficiência - PCD)

    IQVIA
    São Paulo - SP

    Somente PCD - TMF Quality Project Manager or Records Mgmt Analyst Full home-based (LATAM) Job Overview Serve as the liaison between Records Management and user departments regarding Trial Master Files. Apply clinical research records management expertise to provide project-related assistance across multiple projects, sites, and project teams. Ensure all work is conducted in accordance with Standard Operating Procedures (SOPs), policies, practices, Good Clinical Practice (GCP), and applicable regulatory requirements, while meeting quality and timeline metrics. May lead teams functionally, where assigned, including awareness of scope of work, budget, and available resources. Essential Functions Ensure project timelines are met and facilitate the orderly transfer, imaging, scanning, retention, and disposition of project-related and business records.Ensure all work is conducted in accordance with SOPs, policies, practices, Good Clinical Practice (GCP), and applicable regulatory requirements, and meets quality and timeline metrics.Coordinate the retrieval of records requested by users and prepare closed studies for transfer to final destinations within agreed timelines.Monitor filing accuracy and compliance with IQVIA or customer file plans and Standard Operating Procedures (SOPs).Conduct and manage imaging and scanning processes, and train staff on applicable imaging and scanning procedures.Maintain records center security to protect record integrity by ensuring compliance with SOPs.Interface with internal departments to support retrieval projects and ensure information needs are met.Train team members on records management tasks, policies, and procedures.Serve as the primary point of contact for internal and external clients.Coordinate the transfer, recall, and disposition of records to commercial records storage centers.Oversee the disposal of obsolete records and ensure efficient maintenance of records storage space, supplies, and equipment.Assist management with the implementation of strategic goals, plans, cost proposals, and resource projections for records management projects.May function as team leader for records management projects.Qualifications Bachelor’s degree in Records Management or a related field, or equivalent combination of education, training, and experience.Minimum of four (4) years of experience working in a technically related records management environment.Prior experience with Trial Master File (TMF) oversight, review and/or reconciliation across clinical studiesStrong knowledge of applicable research and regulatory requirements, including International Council for Harmonization (ICH), Good Clinical Practice (GCP), and relevant local laws, regulations, and guidelines.Working knowledge of technology applications relevant to records management environments.Ability to identify and analyze problems, develop effective solutions, and make sound decisions.Demonstrated ability to manage multiple tasks and projects within defined timelines while balancing competing priorities.Strong attention to detail and ability to remain focused under pressure.Excellent organizational, planning, and decision-making skills.Strong written and verbal communication skills, including a solid command of the English language.Ability to establish and maintain effective working relationships with internal and external clients.Demonstrated ability to lead and guide others. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

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    Vaga PCD Clinical Trial Manager - Sponsor Dedicated (Pessoa Com Deficiência - PCD)

    IQVIA
    São Paulo - SP

    Somente PCD - Clinical Trial Manager – Sponsor Dedicated. Clinical Project Management services provide management of a clinical trial (s) in a local level. Services/deliverables include operational oversight of assigned project(s) at the local level for end-to-end project management from start-up through to closeout activities. Tasks & Responsibilities: • Services rendered will adhere to applicable Sponsor SOPs, WIs, policies, codes of Good Clinical Practice (GCP), local regulatory requirements. • Prepares or contributes to high level budget estimate in response to Request for Service’s followed by detailed budget proposal. Ensures overall contract management, including review and approval of external service provider (ESP) contracts, change orders and ensures services are delivered per contract. • Act as primary company contact for assigned trial at the country level and ensures local/country team is tracking project progress against planned timelines and monitors patient recruitment rate to ensure that target enrollment will be met across the allocated countries. This may require development of local trial specific procedures and tools, recruitment planning, contingency and risk management, and budget forecasting. • Drive study compliance by maintaining and updating trial management systems, using study tools and management reports available to analyze trial progress. Participates in preparation for and conduct of Health Authority (HA) inspections and internal Quality Assurance audits. Escalates corrective and preventive actions (CAPA) to GTL MAO and CPL when the trial deviates from plans and communicates study progress and issues to study management teams and business partners. • Contributes to site level recruitment strategy and contingency planning and implementation in partnership with other functional areas to achieve clinical research target. • Contributes to patient understanding of protocol and patient safety by contributing to the review of country specific informed consent in accordance with procedural document/templates. This includes reviewing and managing site specific informed consent forms in accordance with SOPs, other procedural documents and applicable regulations. Essentials Requirements: • BA/BS degree. • Degree in a health or science related field. • Minimum of 2 years of local/regional trial management experience in the pharmaceutical industry or CRO and previous experience as Clinical Research Associate. • Specific therapeutic area experience may be required depending on the position. • Strong working knowledge of ICH-GCP, company standard operating procedures, local laws and regulations, assigned protocols and associated protocol specific procedures. • Strong IT skills in appropriate software and company systems. Willingness to travel with occasional overnight stay away from home according to business needs. • Excellent decision-making and string financial management skills. • Proficient in speaking and writing the country language and English. Good written and oral communication skills as appropriate. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

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    Vaga PCD Senior Site Contracts Associate (Pessoa Com Deficiência - PCD)

    IQVIA
    São Paulo - SP

    Somente PCD - IQVIA Biotech is hiring for Sr. Site Contracts Associate in Brazil with 5 years experience negotiating clinical site contracts and budget templates. IQVIA Biotech is a full-service CRO purpose-built to serve biotech sponsors. With over 25 years of experience, we offer agile, therapeutically aligned solutions and trusted partnerships that help bring breakthrough treatments to patients faster. Job Overview Develop the global contracting strategy and support the delivery of all required start-up contracting activities for selected sponsors, studies or multi-protocol programs as determined by the Sponsor’s requirements. Essential Functions • Develop Coordinate the development of investigator grants and estimates, contracting strategies and proposal text to support the proposal development process. • Develop contract language, payment language and budget templates as required as applicable to the position • Utilize and maintain contracting systems, tools, processes, and training materials for selected sponsors, studies or multi-protocol programs according to the Scope of Work and Project Plan, within the agreed project strategy. • Ensure collaboration, including communication with sponsors, stakeholders and RSU regions and countries as applicable to the position, to successfully deliver the agreed project scope in compliance with sponsor requirements and/or the RSU Management Plan. • Provide specialist legal, operational and financial contracting support to the Study Teams, as applicable to site agreements to facilitate efficient business development and initiation and maintenance of clinical trials, whilst enabling compliance with regulatory requirements. • Assist with the creation and/or review of core scientific, technical and administrative documentation to support business development and enable study initiation and maintenance, as required. • Contribute to the collection, interpretation, analysis and dissemination of accurate contracting intelligence to support assigned studies and the wider company, as required. • Ensure overall contracting efficiency and adherence to project timelines and financial goals as applicable to site agreements • Report contracting performance metrics and out of scope contracting activities as required. • Work with Quality Management to ensure appropriate contract management and quality standards. Mentor and coach colleagues as required including the delivery of training materials as required. Qualifications • Bachelor's Degree Related field. • 3-5-year relevant sponsor or clinical research organization clinical site contracting experience, including demonstrable global and/or regional experience acting as a contract negotiator. Equivalent combination of education, training and experience. • Good negotiating and communication skills with ability to challenge. • Strong legal, financial and/or technical writing skills. • Strong understanding of regulated clinical trial environment and knowledge of drug development process. • Knowledge and ability to apply GCP/ICH and applicable regulatory guidelines. • Knowledge of applicable regulatory requirements, SOPs and company’s Corporate Standards. • Good understanding of clinical trial contract management. • Ability to develop and suggest alternate contracting language, terms, and financial options. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

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    Assistente administrativo de pesquisa clínica (Pessoa Com Deficiência - PCD)

    IQVIA
    São Paulo - SP

    Somente PCD - Visão Geral da Vaga Realizar atividades administrativas diárias, em conjunto com os times de Monitores de Pesquisa Clínica (CRA) e de Regulatórios e Início de Estudos (RSU), para garantir a entrega completa e precisa do Arquivo Mestre do Estudo (TMF). Responsabilidades Essenciais Auxiliar os Monitores de Pesquisa Clínica (CRA) e o time de Regulatórios e Início de Estudos (RSU) na atualização e manutenção precisa de documentos clínicos e sistemas (ex.: Arquivo Mestre do Estudo - TMF) que acompanham a conformidade e desempenho dos centros dentro dos prazos do projeto. Apoiar o time clínico na preparação, manuseio, distribuição, arquivamento e armazenamento de documentação e relatórios clínicos, conforme o escopo de trabalho e os procedimentos operacionais padrão. Auxiliar na revisão periódica dos arquivos do estudo para garantir sua completude. Apoiar os CRAs e RSU na preparação, manuseio e distribuição de materiais do estudo clínico e na manutenção das informações de rastreamento. Auxiliar no rastreamento e gerenciamento dos Formulários de Relato de Caso (CRFs), dúvidas e fluxo de dados clínicos. Atuar como contato central para o time clínico em comunicações, correspondências e documentação relacionada ao projeto designado. Pode acompanhar os CRAs em visitas aos centros para auxiliar nas atividades de monitoramento clínico, após a conclusão do treinamento necessário. Qualificações Graduação em áreas da saúde (preferencialmente). Experiência de 1 ano em ambiente de saúde ou combinação equivalente de educação, treinamento e experiência. Outras experiências administrativas são altamente valorizadas. Inglês em nível intermediário superior. Modelo híbrido de trabalho: escritório localizado em São Paulo, SP. Por favor, envie seu currículo e laudo médico ao se candidatar.

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    Assistente de Recrutamento e Seleção (Pessoa Com Deficiência - PCD)

    IQVIA
    São Paulo - SP

    Somente PCD - Job Overview Localização: São Paulo, Brasil Modelo de trabalho: Híbrido Tipo de contratação: Tempo integral Como Assistente de Recrutamento e Seleção (Talent Acquisition Assistant), você dará suporte às atividades de recrutamento em toda a América Latina, trabalhando em parceria com recrutadores e stakeholders para garantir uma experiência positiva aos candidatos e processos de contratação eficientes. A função combina coordenação de recrutamento, inteligência de mercado de talentos, apoio em busca de candidatos (sourcing) e atividades administrativas. Principais Responsabilidades Apoiar as operações de recrutamento e manter dados e relatórios de candidatos atualizados e precisos. Coletar informações sobre o mercado de talentos e feedback de novos colaboradores na América Latina, com foco no Brasil. Coordenar entrevistas e gerenciar o agendamento entre candidatos e equipes contratantes. Apoiar iniciativas de busca de talentos por meio do LinkedIn e outros canais de recrutamento. Auxiliar na divulgação de vagas, ações de marca empregadora (employer branding) e atividades de atração de talentos. Fornecer suporte administrativo geral à equipe de Talent Acquisition. Qualificações Graduação em Recursos Humanos, Psicologia, Administração de Empresas, Comunicação ou área relacionada. Experiência prévia em recrutamento, coordenação de aquisição de talentos, atividades administrativas ou funções de atendimento ao cliente será considerada um diferencial. Forte capacidade de organização e atenção aos detalhes. Experiência com Microsoft Office, plataformas ATS (Applicant Tracking System) ou LinkedIn será considerada um diferencial. Nível intermediário de inglês e/ou espanhol. Boas habilidades de comunicação e trabalho em equipe.

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    Banco de talentos (Pessoa Com Deficiência - PCD)

    IQVIA
    São Paulo - SP

    Somente PCD - Se você é PCD e tem interesse em fazer parte de nosso time envie o seu currículo para o nosso banco de talentos exclusivo para PCD. Se você não achou nenhuma vaga para PCD com seu perfil nesse momento, não tem problema. Queremos te conhecer melhor e receber seu currículo, inscreva-se por aqui!

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    Perguntas frequentes

    A IQVIA contrata PCD?

    Sim. Nesta atualização (23/09/2026) há 57 vagas da IQVIA para pessoas com deficiência, em São Paulo - SP.

    Como me candidatar às vagas PCD da IQVIA?

    Abra a vaga e siga para a página oficial no PCD Online, onde ficam os requisitos e a candidatura. Tenha em mãos o laudo médico atualizado com o CID.

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