
Clinical Research Monitor-TIPS-3 PHRI Study
6 days ago
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.
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