Senior Oncology Clinical Research Coordinator
Há 5 dias
Job Overview We are seeking a highly skilled and detail-oriented Clinical Research Associate to join our team. The ideal candidate will have experience in conducting Phase 2 clinical trials, with a strong understanding of Good Clinical Practice (GCP), FDA regulations, and ICH guidelines. The CRA will be responsible for monitoring and managing clinical trials, ensuring compliance with regulatory standards, and collaborating with investigators, site personnel, and cross-functional teams. 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
Há 6 dias
Brazil 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), and...
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Contract Clinical Research Associate
Há 5 dias
Brazil 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), and...
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Contract Clinical Research Associate
Há 7 dias
Brazil 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), and...
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Contract Clinical Research Associate
Há 7 dias
Brazil, BR 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), and...
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Senior Clinical Research Associate I
Há 13 horas
Brazil-Remote Parexel Tempo inteiro R$60.000 - R$120.000 por anoWhen our values align, there's no limit to what we can achieve. At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do.Each of us, no matter what we do at...
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Contract Clinical Research Associate
Há 6 dias
Brazil 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 someone...
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Contract Clinical Research Associate
Há 5 dias
Brazil 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 someone who...
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Contract Clinical Research Associate
Há 7 dias
Brazil 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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Epilepsy Research Professional
Há 5 dias
Brazil beBeeClinical Tempo inteiroSenior Clinical Research Associate Position - Epilepsy Study This is an exciting opportunity for experienced Clinical Research Associates to join a Phase II/III Epilepsy Study in the Central and Eastern U.S. The ideal candidate will have at least 5+ years of independent monitoring experience and prior seizure trial experience is strongly desired. We are...
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Contract Clinical Research Associate
Há 3 horas
Brazil, BR 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 Brazil — and it’s available for an immediate start.If you’re someone who thrives in...
