Clinical Research Monitor
About the Role
Roles & Responsibilities:
• Monitor clinical research studies to ensure compliance with approved protocols and GCP guidelines
• Conduct site monitoring visits and review clinical trial documentation
• Verify source data, case report forms, and study records for accuracy and completeness
• Ensure patient safety, data integrity, and regulatory compliance
• Coordinate with investigators, clinical research coordinators, and study teams
• Prepare monitoring reports and follow up on corrective and preventive actions
• Support audits, inspections, and regulatory submissions
• Perform other duties assigned by the principal investigator or authority
• Qualification:
• B.Sc, B.Pharm, M.Sc, M.Pharm, Post Graduation
Age Limit:
• Minimum age: 21 years
• Maximum age: 50 years
Walk-in Interview Details:
• Date: 05-02-2026
• Venue: Mahamana Pandit Madan Mohan Malviya Cancer Centre, Sunder Bagiya, B.H.U Campus, Varanasi, Uttar Pradesh – 221005
About the Organisation:
Tata Memorial Centre (TMC) is a premier institution under the Department of Atomic Energy, Government of India, committed to excellence in cancer care, research, and education, conducting high-quality clinical and translational research across India.
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