Job Description
About the Role
Key Responsibilities
- Lead and manage clinical trial activities from start-up to close-out, ensuring timelines and quality standards are met.
- Coordinate with internal teams and external partners (CROs, vendors, investigators) to ensure smooth trial execution.
- Oversee site selection, initiation, monitoring, and management.
- Ensure compliance with GCP, ICH guidelines, and local regulatory requirements.
- Manage trial budgets, timelines, and risk mitigation plans.
- Review and approve essential documents including protocols, informed consent forms, and study reports.
- Provide regular updates to stakeholders and contribute to cross-functional meetings.
- Support audit readiness and regulatory inspections.
Qualifications
- Bachelor's or advanced degree...