Clinical specialist

JD 1: Clinical Study Management Support Specialist

Role: Clinical Study Management Support Specialist

Responsibilities:

Support global clinical studies across start-up, conduct, and close-out phases. Maintain study trackers, reports, and study documentation. Coordinate with CROs and vendors to ensure study deliverables. Manage TMF and study-related documents. Track study progress, metrics, and compliance issues. Ensure adherence to ICH-GCP, SOPs, and regulatory requirements.

Must-Have Skills:

Clinical Trial Operations Study Management Support TMF Management CRO/Vendor Coordination ICH-GCP Knowledge Documentation & Reporting Communication Skills