- Assist senior team members in the coordination of ongoing clinical trials at assigned sites.
- Undergo comprehensive training in monitoring processes and Good Clinical Practice (GCP).
- Schedule and conduct monitoring visits to clinical trial sites in accordance with the study protocol and regulatory requirements.
- Provide training to site personnel on GCP guidelines and specific study-related activities to ensure compliance.
- Ensure accurate and timely documentation of monitoring visits and maintain detailed records in line with trial protocols.
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Brief Description about the Project · Drug Based Clinical Trial · Clinical Research Monitor · No. of Vacancy:One · Preferred Qualifications: MBBS /BVSc /BDS /MPHW + Post Graduate Degree, including the Integrated PG Degrees. Graduate or Post Graduation with a Diploma in Clinical R ...
Bengaluru, Karnataka5 days ago
Clinical Research Monitor-TIPS-3 PHRI Study - Bengaluru / Bangalore - St Johns Research Institute Sjri
Description
Roles and Responsibilities:
Site Coordination
Training & Development
Monitoring Activities
Site Support
Documentation & Reporting
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Clinical Research Monitor
Only for registered members Bengaluru, Karnataka
