Clinical Research Coordinator

Roles & Responsibilities:
• Coordinate and manage clinical research studies as per approved protocols
• Support investigators in study start-up, patient recruitment, and follow-up activities
• Ensure informed consent process and protocol compliance
• Maintain clinical trial documentation, source documents, and case report forms
• Coordinate with investigators, sponsors, and regulatory authorities
• Monitor data quality, timelines, and study milestones
• Ensure compliance with GCP guidelines, ethical standards, and regulatory requirements
• Assist in audits, inspections, and reporting activities
• Perform other duties assigned by the principal investigator

Qualification:
• M. Sc
• M. Pharm

Age Limit:
• Minimum age: 21 years
• Maximum age: 35 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:
ACTREC is a premier oncology research and education institution under the Tata Memorial Centre, dedicated to advancing cancer research, clinical trials, and patient care through high-quality translational and clinical research programs across India.

Official Notification Click Here