About the role
Position Summary
A Clinical Trial Manager with 3-8 years of experience in the planning, execution, oversight, and delivery of clinical trials in accordance with protocol requirements, ICH-GCP guidelines, applicable regulations, and company SOPs. Manages study timelines, vendors, budgets, and cross-functional teams to ensure high-quality trial conduct and successful study outcomes.
Key Responsibilities
- Manage day-to-day operational aspects of Phase I–III clinical trials from study start-up through closeout.
- Develop and maintain study timelines, project plans, and trial tracking tools.
- Coordinate activities among CROs, clinical sites, vendors, and internal stakeholders.
- Monitor study progress and identify risks, implementing mitigation strategies as needed.
- Review and execute according to essential study documents, including protocols, informed consent forms, monitoring plans, and study manuals.