Clinical Trials Coordinator

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...

Job Opportunity: Phase 2 Clinical Trials Monitor We are seeking a detail-oriented and experienced Clinical Research Associate (CRA) to monitor and manage 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...

Job Opportunity: Phase 2 Clinical Trials MonitorWe are seeking a detail-oriented and experienced Clinical Research Associate (CRA) to monitor and manage 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...

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...

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...

Senior Clinical Data Science Programmer About the Role: This is a pivotal position in developing and implementing programming solutions to support the analysis and reporting of clinical trial data. You will contribute to the advancement of innovative treatments and therapies by ensuring the accuracy and efficiency of data processing through your programming...

Senior Clinical Data Science ProgrammerAbout the Role:This is a pivotal position in developing and implementing programming solutions to support the analysis and reporting of clinical trial data.You will contribute to the advancement of innovative treatments and therapies by ensuring the accuracy and efficiency of data processing through your programming...

**Are you a Registered Nurse interested in Clinical Trial work?** IQVIA is looking for qualified Registered Nurses interested in community and clinical trial work to visit clinical trial patients in their homes. You will be responsible for going to patient homes to assist with conducting research, collecting data and samples to help evaluate safety/efficacy...

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...