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3 semanas atrás


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Project Manager Clinical Research Associate role available. The successful candidate will be responsible for ensuring a clinical 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. This detail-oriented and experienced CRA will monitor and manage Phase 2 Seizure study clinical trials. The following key responsibilities are involved: Site Management and Monitoring: Conduct site qualification, initiation, interim monitoring, and close-out visits. Ensure proper site adherence to protocols, GCP, and regulatory requirements. Regulatory Compliance: Ensure all clinical trial documentation is maintained according to regulatory guidelines. Review informed consent documents and confirm proper consenting procedures. Safety and Data Management: Monitor and report adverse events (AEs), serious adverse events (SAEs), and dose-limiting toxicities. To qualify for this role, you must have: 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. Benefits This opportunity offers a challenging and rewarding work environment with opportunities for growth and development. If you are a motivated and detail-oriented professional looking for a new challenge, we encourage you to apply.



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