Clinical Trial Coordinator (Site Side)

Stellenbeschreibung

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.