Clinical Specialist

Job description

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