Contract Clinical Research Associate
Há 9 horas
Contract CRA Project - 40 hours per week 1 year contract. Seizure or Epilepsy - CNS Job Summary: We are seeking a detail-oriented and experienced Clinical Research Associate (CRA) to monitor and manage Phase 2 Seizure study clinical trials. The CRA will ensure the trial is conducted in compliance with regulatory standards, Good Clinical Practice (GCP), and the study protocol. This position involves collaborating with investigators, site personnel, and cross-functional teams to ensure the safety and well-being of participants in early-phase clinical trials. Key Responsibilities: Site Management and Monitoring: Conduct site qualification, initiation, interim monitoring, and close-out visits. Ensure proper site adherence to protocols, GCP, and regulatory requirements. Verify and ensure accurate data collection and reporting. Assess site performance and provide corrective actions if necessary. Regulatory Compliance: Ensure all clinical trial documentation is maintained according to regulatory guidelines. Review informed consent documents and confirm proper consenting procedures. Collaborate with regulatory teams to ensure timely submissions and approvals. Safety and Data Management: Monitor and report adverse events (AEs), serious adverse events (SAEs), and dose-limiting toxicities. Validate source data and resolve data discrepancies. Ensure timely and accurate documentation of clinical trial data in electronic data capture (EDC) systems. Collaboration and Communication: Build and maintain relationships with study investigators and site staff. Communicate study updates and findings to study sponsors and internal teams. Provide training to site personnel on study protocols, procedures, and GCP compliance. Qualifications: Bachelor’s degree in Life Sciences , Nursing , or a related field. At least 2-4 years of experience as a Clinical Research Associate in oncology trials, with preference for Phase 2 experience. Strong knowledge of Good Clinical Practice (GCP) , FDA regulations, and ICH guidelines. Experience with electronic data capture (EDC) systems and clinical trial management systems (CTMS). Excellent organizational, problem-solving, and communication skills. Preferred Qualifications: Previous experience in early-phase oncology trials (e.g., dose escalation studies, first-in-human trials). Strong understanding of pharmacokinetics (PK) and pharmacodynamics (PD) assessments. Certification as a Clinical Research Professional (CCRA) is a plus.
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Contract Clinical Research Associate
36 minutos atrás
Brasil Barrington James Tempo inteiroContract CRA Project - 40 hours per week 1 year contract. Seizure or Epilepsy - CNS Job Summary: We are seeking a detail-oriented and experienced Clinical Research Associate (CRA) to monitor and manage Phase 2 Seizure study clinical trials. The CRA will ensure the trial is conducted in compliance with regulatory standards, Good Clinical Practice (GCP),...
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Contract Clinical Research Associate
Há 15 horas
Brasil Barrington James Tempo inteiroSenior Clinical Research Associate (CRA) — Epilepsy Study (Phase II/III) I’m currently looking for experienced Senior CRAs to join an exciting Phase II/III Epilepsy Study with one of my key clients. This is a 1.0 FTE contract role supporting 6–8 sites across the Central and Eastern U.S. — and it’s available for an immediate start . If you’re...
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Freelance Clinical Research Associate
4 semanas atrás
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 clinical research associate
3 semanas atrás
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 Clinical Research Associate
4 semanas atrás
Índio do 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:...
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Freelance Clinical Research Associate
3 semanas atrás
Índio do 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:...
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UX Research Analyst
4 semanas atrás
Brasil Pulse Labs Tempo inteiroThis is a 3-month contract role. Contract extension is not guaranteed, but may occur dependent on performance, company work volume, and budget. Pulse Labs is empowering insights and elevating experiences for the world's top technology companies. Backed by investors including Google and Amazon, we're revolutionizing product development delivering...
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UX Research Analyst
4 semanas atrás
Índio do Brasil Pulse Labs Tempo inteiroThis is a 3-month contract role. Contract extension is not guaranteed, but may occur dependent on performance, company work volume, and budget. Pulse Labs is empowering insights and elevating experiences for the world's top technology companies. Backed by investors including Google and Amazon, we're revolutionizing product development delivering...
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Business analyst
2 semanas atrás
Brasil Ampstek Tempo inteiroRole :: Business Analyst - Clinical trials or life sciences Location: Brazil/Remote Duration: Long Term Contract Key Responsibilities: Understand and document business and data requirements across clinical domains and translate them into actionable technical tasks Manage and maintain Jira boards for the Data Engineering team: groom stories, track progress,...
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Research Drive Assistant
Há 15 horas
Brasil Pulse Labs Tempo inteiroShort term contract, Dec 1-23 Pulse Labs is empowering insights and elevating experiences for the world's top technology companies. Backed by investors including Google and Amazon, we're revolutionizing product development delivering human-centered, actionable insights at every stage of the product lifecycle from inception to market release and beyond. We...
