Key Responsibilities:
- Assist clinical project managers in planning and executing clinical trials
- Support project tracking, timelines, and deliverables
- Maintain and update project documentation and Trial Master File (TMF)
- Coordinate with cross-functional teams including CRAs, data management, and regulatory teams
- Prepare project status reports and dashboards
- Support study start-up, conduct, and close-out activities
- Ensure compliance with protocols, SOPs, GCP, and regulatory guidelines
- Assist in organizing meetings, preparing agendas, and documenting minutes