Contract Clinical Research Associate
Há 2 dias
Contract CRA Project - 40 hours per week 1 year contract.Seizure or Epilepsy - CNSJob Summary: We are seeking a detail-oriented and experiencedClinical Research Associate (CRA)to monitor and managePhase 2 Seizure studyclinical 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 inLife Sciences,Nursing, or a related field. At least2-4 yearsof experience as a Clinical Research Associate in oncology trials, with preference forPhase 2experience. Strong knowledge ofGood Clinical Practice (GCP),FDAregulations, andICHguidelines. Experience with electronic data capture (EDC) systems and clinical trial management systems (CTMS). Excellent organizational, problem-solving, and communication skills.Preferred Qualifications: Previous experience inearly-phase oncology trials(e.g., dose escalation studies, first-in-human trials). Strong understanding of pharmacokinetics (PK) and pharmacodynamics (PD) assessments. Certification as aClinical Research Professional (CCRA)is a plus.
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Contract Clinical Research Associate
Há 12 horas
Brasília, 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 3 dias
Brasília, Brasil Barrington James Tempo inteiroContract CRA Project - 40 hours per week 1 year contract. Seizure or Epilepsy - CNSJob Summary: We are seeking a detail-oriented and experiencedClinical Research Associate (CRA)to monitor and managePhase 2 Seizure studyclinical trials. The CRA will ensure the trial is conducted in compliance with regulatory standards, Good Clinical Practice (GCP), and the...
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Contract Clinical Research Associate
1 dia atrás
Brasília, DF, 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), and...
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Contract Clinical Research Associate
Há 2 dias
Brasília, Brasil Barrington James Tempo inteiroSenior Clinical Research Associate (CRA) — Epilepsy Study (Phase II/III) I’m currently looking for experiencedSenior CRAsto join an excitingPhase II/III Epilepsy Studywith one of my key clients. This is a1.0 FTE contract rolesupporting 6–8 sites across theCentral and Eastern U.S.— and it’s available for animmediate start.If you’re someone who...
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Clinical Research Associate – South America
2 semanas atrás
Brasília, Brasil Resourcing Life Science Tempo inteiroCompany Description Our client is a Global CRO currently supporting various Pharmaceutical & Biotech companies globally. They offer a full service solution encompassing clinical & non-clinical development, peri-approval & market access. They are currently seeking a CRA / Clinical Research Associate Job Overview Monitoring clinical studies in phases II-III...
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Freelance clinical research associate
4 semanas atrás
Brasília, 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 BrazilHours: 1 x 0.35 FTE and 1 x 0.6 FTEStart: ASAPDuration: 6...
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Freelance Clinical Research Associate
4 semanas atrás
Brasília, DF, 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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Clinical Trial Specialist
1 semana atrás
Brasília, Brasil beBeeClinicalResearch Tempo inteiroClinical Research Associate Role We are seeking a skilled Clinical Research Associate to support Phase 2 and 3 clinical trials in Brazil. This is an exciting opportunity for a professional to lead site visits, ensure compliance and data integrity, and collaborate with investigators and internal teams. Conduct site evaluations, initiations, monitoring &...
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Senior Clinical Research Associate I
Há 2 dias
Brasília, Brasil Parexel Tempo inteiro**Parexel FSP is hiring multiple Sr CRAs in Brazil!** The Senior Clinical Research Associate (Sr. CRA) is responsible for the site management, site monitoring and close-out of assigned clinical trials investigator sites to ensure patient safety and quality study execution in accordance with applicable prevailing laws, Good Clinical Practices (GCP), and the...
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Site Contract Specialist
2 semanas atrás
Brasília, Brasil Alimentiv Tempo inteiroThe Site Contract Specialist will be responsible for the execution, negotiation and administration of assigned site contracts and supporting documents including, confidentiality agreements, clinical trial agreements, letters of indemnity and authorization. The incumbent will coordinate with sites, sponsors, vendors and internal stakeholders to facilitate the...
