Clinical Research Coordinator
About the Role
Roles & Responsibilities:
• Coordinate and manage clinical research studies as per approved protocols
• Assist investigators in study initiation, patient recruitment, and follow-up
• Ensure informed consent process and protocol adherence
• Maintain clinical trial documentation, source data, and case report forms
• Coordinate with investigators, sponsors, ethics committees, and regulatory teams
• Monitor study timelines, data quality, and compliance
• Support audits, inspections, and reporting activities
• Perform other duties assigned by the principal investigator
Qualification:
• B.Sc, B.Pharm, M.Sc, M.Pharm, Post Graduation in relevant discipline
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, dedicated to cancer treatment, research, and education, conducting high-quality clinical research to improve cancer care and outcomes across the country.
Official Notification Click Here
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