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