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