191 vagas para pessoas com deficiência, atualizadas em 25/09/2026
Emprego PCD em São Paulo: resumo das vagas abertas
Há 191 vagas para pessoas com deficiência em São Paulo, de 33 empresas, entre elas IQVIA, Viveo e C&A. As áreas com mais oportunidades são Saúde, Comercial e Logística. Confira os detalhes por aqui e conclua a candidatura com segurança na página oficial da vaga no PCD Online.
Câmara de Comercialização de Energia Elétrica - CCEE (12)
Arcolimp (8)
BRQ Digital Solutions (6)
Tipo de contrato
CLT (167)
Home Office (13)
Estágio (11)
Vagas PCD abertas em São Paulo
CLT
Vaga PCD Analista Fiscal Pleno - Apuração/Parametrização | Viveo | São Paulo - SP (Pessoa Com Deficiência - PCD)
Viveo
SAO PAULO, São Paulo
Somente PCD - VIVEO - Cuidar de cada vida, simples assim! Fundados em 1996, somos líderes na fabricação e na distribuição de materiais e medicamentos para o segmento da saúde, com produtos e soluções para todo o Brasil. Com capital 100% nacional, com mais de 50 unidades operacionais e centros de distribuição em todas as regiões do país, temos nossa própria frota e contamos com mais de 6.500 colaboradores diretos. Com o propósito de cuidar de cada vida, somos a única empresa do Brasil que atua de forma completa no mercado da saúde. Essa atuação reforça nosso compromisso em oferecer soluções confiáveis, ágeis e inovadoras ao setor – incluindo fabricação, distribuição, gestão de estoque, transporte e soluções personalizadas aos hospitais, clínicas, laboratórios, farmácias, atacados, indústrias farmacêuticas e aos pacientes finais. Buscamos encontrar e viabilizar as inovações que definirão como cuidar das pessoas do amanhã.
Vaga PCD Advogado Tributário Jr | Viveo | São Paulo - SP (Pessoa Com Deficiência - PCD)
Viveo
SAO PAULO, São Paulo
Somente PCD - VIVEO - Cuidar de cada vida, simples assim! Fundados em 1996, somos líderes na fabricação e na distribuição de materiais e medicamentos para o segmento da saúde, com produtos e soluções para todo o Brasil. Com capital 100% nacional, com mais de 50 unidades operacionais e centros de distribuição em todas as regiões do país, temos nossa própria frota e contamos com mais de 6.500 colaboradores diretos. Com o propósito de cuidar de cada vida, somos a única empresa do Brasil que atua de forma completa no mercado da saúde. Essa atuação reforça nosso compromisso em oferecer soluções confiáveis, ágeis e inovadoras ao setor – incluindo fabricação, distribuição, gestão de estoque, transporte e soluções personalizadas aos hospitais, clínicas, laboratórios, farmácias, atacados, indústrias farmacêuticas e aos pacientes finais. Buscamos encontrar e viabilizar as inovações que definirão como cuidar das pessoas do amanhã.
Vaga PCD Analista Fiscal Pleno - Fechamento e Obrigações Acessórias | Viveo | São Paulo - SP (Pessoa Com Deficiência - PCD)
Viveo
SAO PAULO, São Paulo
Somente PCD - VIVEO - Cuidar de cada vida, simples assim! Fundados em 1996, somos líderes na fabricação e na distribuição de materiais e medicamentos para o segmento da saúde, com produtos e soluções para todo o Brasil. Com capital 100% nacional, com mais de 50 unidades operacionais e centros de distribuição em todas as regiões do país, temos nossa própria frota e contamos com mais de 6.500 colaboradores diretos. Com o propósito de cuidar de cada vida, somos a única empresa do Brasil que atua de forma completa no mercado da saúde. Essa atuação reforça nosso compromisso em oferecer soluções confiáveis, ágeis e inovadoras ao setor – incluindo fabricação, distribuição, gestão de estoque, transporte e soluções personalizadas aos hospitais, clínicas, laboratórios, farmácias, atacados, indústrias farmacêuticas e aos pacientes finais. Buscamos encontrar e viabilizar as inovações que definirão como cuidar das pessoas do amanhã.
Vaga PCD Analista Tributário Jr | Viveo | São Paulo - SP (Pessoa Com Deficiência - PCD)
Viveo
SAO PAULO, São Paulo
Somente PCD - VIVEO - Cuidar de cada vida, simples assim! Fundados em 1996, somos líderes na fabricação e na distribuição de materiais e medicamentos para o segmento da saúde, com produtos e soluções para todo o Brasil. Com capital 100% nacional, com mais de 50 unidades operacionais e centros de distribuição em todas as regiões do país, temos nossa própria frota e contamos com mais de 6.500 colaboradores diretos. Com o propósito de cuidar de cada vida, somos a única empresa do Brasil que atua de forma completa no mercado da saúde. Essa atuação reforça nosso compromisso em oferecer soluções confiáveis, ágeis e inovadoras ao setor – incluindo fabricação, distribuição, gestão de estoque, transporte e soluções personalizadas aos hospitais, clínicas, laboratórios, farmácias, atacados, indústrias farmacêuticas e aos pacientes finais. Buscamos encontrar e viabilizar as inovações que definirão como cuidar das pessoas do amanhã.
Vaga PCD Coordenador(a) de Desenvolvimento TI - Viveo | São Paulo/ SP (Pessoa Com Deficiência - PCD)
Viveo
SAO PAULO, São Paulo
Somente PCD - VIVEO - Cuidar de cada vida, simples assim! Fundados em 1996, somos líderes na fabricação e na distribuição de materiais e medicamentos para o segmento da saúde, com produtos e soluções para todo o Brasil. Com capital 100% nacional, mais de 50 unidades operacionais e centros de distribuição em todas as regiões do país, temos nossa própria frota e contamos com mais de 6.500 colaboradores diretos. Com o propósito de cuidar de cada vida, somos a única empresa do Brasil que atua de forma completa no mercado da saúde. Essa atuação reforça nosso compromisso em oferecer soluções confiáveis, ágeis e inovadoras ao setor – incluindo fabricação, distribuição, gestão de estoque, transporte e soluções personalizadas aos hospitais, clínicas, laboratórios, farmácias, atacados, indústrias farmacêuticas e aos pacientes finais. Buscamos encontrar e viabilizar as inovações que definirão como cuidar das pessoas do amanhã. Saiba mais em: https://www.viveo.com.br/ ;
Vaga PCD Técnico de Segurança do Trabalho | CD - Raposo Tavares (Pessoa Com Deficiência - PCD)
C&A
SAO PAULO, São Paulo
Somente PCD - Trabalhamos para você ser mais você em todos os momentos, começando pela sua carreira Referência no varejo de moda, a C&A se orgulha de ter mais de 14 mil pessoas atuando em suas operações no Brasil para oferecer a melhor experiência para nossas clientes! Trabalhar na C&A é fazer parte de um ambiente inovador e divertido, que estimula o desenvolvimento profissional em todas as fases da carreira. Aqui você pode ser quem é! O respeito às pessoas e à diversidade fazem parte dos nossos valores. Enxergamos a moda como uma plataforma de expressão e de como as pessoas se conectam. Queremos fazer uma moda com impacto positivo, o que nos torna únicos. Nossa cultura acredita no valor e na riqueza das diferenças. Somos uma multinacional com alma brasileira. Curta nossa página de carreira no Linkedin para saber mais sobre nosso dia-a-dia! Se você se identifica com a C&A e procura uma empresa, acima de tudo, apaixonada por pessoas, #VemPraCeA.
Vaga PCD RFI Developer 2 (Pessoa Com Deficiência - PCD)
IQVIA
SAO PAULO, São Paulo
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.
Vaga PCD Regional Specialist in Argentina or Brazil (Pessoa Com Deficiência - PCD)
IQVIA
SAO PAULO, São Paulo
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.
Vaga PCD Pharmacovigilance Specialist (Fluent in English + Italian) (Pessoa Com Deficiência - PCD)
IQVIA
SAO PAULO, São Paulo
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.
Vaga PCD Clinical Scientist in CNS - LATAM (Pessoa Com Deficiência - PCD)
IQVIA
SAO PAULO, São Paulo
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.
Vaga PCD (Senior) Data Team Lead (Pessoa Com Deficiência - PCD)
IQVIA
SAO PAULO, São Paulo
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
Vaga PCD PMO – Project Manager (Pessoa Com Deficiência - PCD)
IQVIA
SAO PAULO, São Paulo
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.
Vaga PCD RWE - Site Mgr 2 (Pessoa Com Deficiência - PCD)
IQVIA
SAO PAULO, São Paulo
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
Vaga PCD Site Activation Specialist (North America team) (Pessoa Com Deficiência - PCD)
IQVIA
SAO PAULO, São Paulo
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.
Vaga PCD Sr. Contract Negotiation Specialist (North America team) (Pessoa Com Deficiência - PCD)
IQVIA
SAO PAULO, São Paulo
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.
Vaga PCD Revenue Analyst (Pessoa Com Deficiência - PCD)
IQVIA
SAO PAULO, São Paulo
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.
Vaga PCD Gestor de Operações de Navegação do Paciente (Pessoa Com Deficiência - PCD)
IQVIA
SAO PAULO, São Paulo
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.
Vaga PCD Consultor Navegador (Pessoa Com Deficiência - PCD)
IQVIA
SAO PAULO, São Paulo
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.
Vaga PCD Site Activation Specialist (Pessoa Com Deficiência - PCD)
IQVIA
SAO PAULO, São Paulo
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.
Vaga PCD Centralized Monitoring Lead in LATAM (Remote) (Pessoa Com Deficiência - PCD)
IQVIA
SAO PAULO, São Paulo
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.
Nesta atualização (25/09/2026) há 191 vagas para pessoas com deficiência em São Paulo, publicadas por 33 empresas. O número muda todos os dias, conforme as empresas abrem e encerram processos seletivos.
Quais áreas mais contratam PCD em São Paulo?
Hoje as áreas com mais vagas PCD em São Paulo são Saúde, Comercial e Logística. Use os links de área nesta página para ver só as vagas de cada uma.
Como me candidatar a uma vaga PCD em São Paulo?
Abra a vaga desejada e siga para a página oficial no PCD Online, onde ficam os requisitos e o botão de candidatura. Tenha em mãos o laudo médico atualizado com o CID, que as empresas pedem para enquadrar a vaga na Lei de Cotas.
Empresas em São Paulo são obrigadas a contratar PCD?
Sim. Pela Lei de Cotas (Lei 8.213/91), empresas com 100 ou mais funcionários em São Paulo - SP devem reservar de 2% a 5% das vagas para pessoas com deficiência ou reabilitadas, sob pena de multa.