Clinical Trial Coordinator (Site Side)

Description du Poste

Responsible for the operational and regulatory implementation of academic and industrial clinical trials within my medical department. My role encompasses the entire study lifecycle: from contract negotiation and budgeting to data management (eCRF) and the execution of protocol-specific tasks that fall outside of medical or nursing duties. I coordinate with various departmental stakeholders to ensure documented processes, rigorous traceability, and strict compliance with international Good Clinical Practice (GCP) guidelines and current healthcare regulations.