Clinical Research Coordinator

Roles & Responsibilities
• Coordinate and manage clinical research studies in accordance with approved protocols
• Assist in patient screening, recruitment, and informed consent processes
• Maintain study documentation, case report forms, and regulatory files
• Ensure compliance with Good Clinical Practice (GCP) and institutional guidelines
• Liaise with investigators, sponsors, ethics committees, and study teams
• Monitor patient visits and follow-up schedules as per trial requirements
• Collect, process, and maintain accurate clinical data

Qualification
• M.Pharm (Master's degree in Pharmacy) / B.Pharm (Bachelor's degree in Pharmacy / B.Sc / M.Sc from a recognized institution
• Post Graduate Diploma in Clinical Research is Mandatory

Experience
• Minimum One Year of Experience in Clinical Research oncology is Mandatory

Skills
• Strong documentation and data management skills
• Excellent communication and coordination abilities
• Attention to detail and regulatory compliance awareness
• Ability to work effectively within a multidisciplinary healthcare team

Age Limit
• Minimum: 21 years
• Maximum: 35 years

About the Organization
Tata Memorial Centre (TMC) is a premier cancer research and treatment institution in India, operating under the Department of Atomic Energy, Government of India. It is dedicated to advancing cancer care, research, and education through high-quality clinical services and innovative research programs.

Walk-in Interview Details
Date: 25-02-2026
Reposting Time: 01:00 P.M. TO 02:00 P.M
Venue: HBB (Homi Bhabha Building), Tata Memorial Hospital, 11th Floor, Room No. 1115, Dr. E. Borges Marg, Parel, Mumbai – 400012