Roles and Responsibilities :
Site Coordination
- Assist senior team members in the coordination of ongoing clinical trials at assigned sites.
Training & Development
Undergo comprehensive training in monitoring processes and Good Clinical Practice (GCP).Monitoring Activities
Schedule and conduct monitoring visits to clinical trial sites in accordance with the study protocol and regulatory requirements.Site Support
Provide training to site personnel on GCP guidelines and specific study-related activities to ensure compliance.Documentation & Reporting
Ensure accurate and timely documentation of monitoring visits and maintain detailed records in line with trial protocols.Skills Required
Site Monitoring, Documentation