CRA 2 - Brazil
Há 6 dias
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. #J-18808-Ljbffr
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Freelance CRA
Há 7 dias
São Paulo, Brasil IQVIA Tempo inteiroJoin IQVIA Biotech as a Freelance CRA supporting Phase 2 and 3 clinical trials. You’ll lead site visits, monitor compliance, and ensure high-quality data—all while working with a passionate team. We currently have two projects in Brazil: Location: Brazil - travel required for both roles across Brazil Hours: 1 x 0.35 FTE and 1 x 0.6 FTE Start: ASAP...
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Freelance CRA
Há 3 dias
São Paulo, São Paulo, Brasil IQVIA Tempo inteiro US$100.000 - US$120.000 por anoJoin IQVIA Biotech as a Freelance CRA supporting Phase 2 and 3 clinical trials. You'll lead site visits, monitor compliance, and ensure high-quality data—all while working with a passionate team.We currently have two projects in Brazil:Location: Brazil - travel required for both roles across BrazilHours: 1 x 0.35 FTE and 1 x 0.6 FTEStart: ASAPDuration: 6...
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São Paulo, Brasil Netvagas Tempo inteiroJoin to apply for the Gerente comercial operacoes estruturadas originacao cri cra e debentures role at Netvagas OverviewEstamos em busca de um(a) Gerente de Operações Estruturadas para atuar com foco em originação de operações no mercado de capitais, especialmente em CRI (Certificados de Recebíveis Imobiliários), CRA (Certificados de Recebíveis do...
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São Paulo, Brasil Netvagas Tempo inteiroJoin to apply for the Gerente comercial operacoes estruturadas originacao cri cra e debentures role at Netvagas Overview Estamos em busca de um(a) Gerente de Operações Estruturadas para atuar com foco em originação de operações no mercado de capitais, especialmente em CRI (Certificados de Recebíveis Imobiliários), CRA (Certificados de Recebíveis do...
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CRA 2 - Brazil
1 semana atrás
São Paulo, Brasil IQVIA Tempo inteiroLocation: 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...
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CRA 2 - Brazil
1 semana atrás
São Paulo, Brasil IQVIA Tempo inteiroLocation 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...
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Cra Ii And Senior Cra
Há 7 dias
São Paulo, Brasil Icon Tempo inteiroCRA II and SR CRA - Remote - Brazil ICON plc is a world-leading healthcare intelligence and clinical research organization.We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.We are currently seeking CRAs II and Senior CRAs to join our...
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In house CRA
2 semanas atrás
São Paulo, São Paulo, Brasil ReSolution Latin America Tempo inteiro R$80.000 - R$120.000 por anoAs part of our continued expansion, ReSolution Latin America, a specialized CRO with operations across the Latin American region is looking for an In house CRA to join our team in Brazil.If you thrive working in a positive, can-do environment where your contribution makes a real difference and want to further your career in an expert and dynamic company...
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CRA 1 - Brazil
2 semanas atrás
São Paulo, Brasil IQVIA Tempo inteiroOverview Join to apply for the CRA 1 - Brazil role at IQVIA 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...
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Cra Ii
2 semanas atrás
São Paulo, SP, Brasil Icon plc Tempo inteiroCRA II for São Paulo, Brazil - Homeworker ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development CRA II JR123930 Site: São Paulo, Brazil We are...
