Clinical Research Monitor-TIPS-3 PHRI Study

7 days ago

Bengaluru, India St Johns Research Institute Sjri Full time

Job Description

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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