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    CLT

    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.

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    CLT

    GESTOR TRANSPORTE (Pessoa Com Deficiência - PCD)

    CMAA - Companhia Mineira de Açúcar e Álcool
    ITUIUTABA, Minas Gerais

    Somente PCD - Planejar, coordenar e supervisionar as atividades da frota de veículos da empresa, garantindo a eficiência e segurança das operações de transporte. Gerenciar a equipe de motoristas, incluindo escalar, acompanhar e avaliar o desempenho. Analisar indicadores de desempenho e custos operacionais da frota, propondo melhorias e soluções para otimização. Realizar a gestão de contratos e relacionamento com fornecedores de serviços de transporte. Elaborar relatórios gerenciais e acompanhar o orçamento da área de transporte. Assegurar o cumprimento de normas, regulamentos e legislação aplicáveis ao transporte.

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    Home Office

    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.

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    CLT

    Auxiliar de Embalagem (Pessoa Com Deficiência - PCD)

    LACTALIS
    ARARAS, São Paulo

    Somente PCD - Venha fazer parte da maior empresa de lácteos do mundo! Estamos em busca de pessoas dedicadas e comprometidas para fazer parte do nosso time na posição de Auxiliar Embalagem. Segue abaixo um resumo dos desafios da posição: Responsável por manter a organização e limpeza do setor, realizar a montagem e paletização de caixas, abastecer máquinas. Também realiza a retirada de materiais e oferece suporte às escalas da equipe. O que esperamos de você: * Ensino fundamental completo. * Experiência prévia em funções operacionais é desejável. * Habilidades de organização e atenção aos detalhes; * Capacidade de cumprir normas internas.. O que oferecemos: - Vale Transporte- Vale Alimentação - Convênio Médico Unimed- Convênio Odontológico- Auxílio Óculos - Auxílio Material Escolar- Auxílio Creche- PLR

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    Home Office

    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.

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    Home Office

    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.

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