Clinical Study Coordinator: Monitoring & Site Operations
Worldwide Clinical Trials
Worldwide Clinical Trials is seeking an Associate Clinical Study Manager to oversee site-level monitoring across multiple trials (Phase I–IV), locally or globally, ensuring timely, quality execution. You will support the CSM, coordinate monitoring visits, collaborate with clinic departments, manage documentation, and ensure compliance with GCP and SOPs. A Life Sciences degree or clinical research experience is required, with at least 1 year as a Clinical Research Coordinator preferred. #J-18808-Ljbffr Worldwide Clinical Trials
Vacancy posted 3 days ago
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