- 5 years of experience as a Clinical Research Coordinator (CRC); or
- A combined 5 years of experience as a Clinical Trial Assistant (CTA) and Clinical Research Associate (CRA).
- Execute all clinical trial activities (PSSV, SIV, Monitoring, Close-out) across projects.
- Ensure full compliance with Protocol, GCP, SOP, ICH-GCP & NDCT 2019.
- Patient Recruitment & Retention
- Data Quality & Regulatory Compliance
- Stakeholder Coordination & Communication
- Team Management & Performance
- Feasibility & Site Expansion
- Patient Safety & Ethics Compliance
- Risk Management & Issue Resolution