Senior Clinical Research Associate

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...

Job Overview:We are seeking a qualified Clinical Research Associate to support Phase 2 and 3 clinical trials in Brazil.As a key team member, you will lead site visits, monitor compliance, and ensure high-quality data.Your Responsibilities:Conduct site evaluations, initiations, monitoring & close-outsEnsure Good Clinical Practice (GCP) compliance and data...

Clinical research associates play a vital role in the healthcare industry, overseeing clinical trials from initiation to completion.Their work involves ensuring compliance with ICH-GCP guidelines and applicable regulations.Key ResponsibilitiesManages study documents according to local regulations and ICH-GCP guidelines.Collaborates with site teams to resolve...

Senior Clinical Research Associate (CRA) This role supports a Phase II/III Epilepsy Study with regular site visits across the United States. Duration: 12 months with potential renewal Experience: At least 5+ years of independent monitoring Travel: Frequent site visits Therapeutic Area: Neurology with strong desire for seizure trial experience The sponsor...

Clinical research associates play a vital role in the healthcare industry, overseeing clinical trials from initiation to completion. Their work involves ensuring compliance with ICH-GCP guidelines and applicable regulations. Key Responsibilities Manages study documents according to local regulations and ICH-GCP guidelines. Collaborates with site teams to...

Senior 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 neurology...

Senior Clinical Research Associate (CRA)This role supports a Phase II/III Epilepsy Study with regular site visits across the United States.Duration: 12 months with potential renewalExperience: At least 5+ years of independent monitoringTravel: Frequent site visitsTherapeutic Area: Neurology with strong desire for seizure trial experienceThe sponsor...

Key Responsibilities: Monitor and manage clinical trials. Ensure site compliance with regulatory requirements. Verify accurate data collection and reporting. Evaluate site performance and implement corrective actions as needed. About the Ideal Candidate: A Bachelor's degree in Life Sciences, Nursing, or a related field is required. At least 2-4 years of...

Join 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. Project Details Location: Brazil – travel required for both roles across Brazil Hours: 1 x 0.35 FTE and 1 x 0.6 FTE Start: ASAP Duration: 6 months Your Role...

We are seeking a detail-oriented and experienced Clinical Research Associate to monitor and manage early-phase clinical trials. The successful candidate 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...