Clinical Trial Coordinator

Roles & Responsibilities
• Coordinate day-to-day clinical trial activities as per study protocols
• Assist Principal Investigator in subject recruitment and screening
• Ensure informed consent process is conducted as per GCP guidelines
• Maintain and update Trial Master File (TMF) and essential study documents
• Coordinate with sponsors, CROs, ethics committees, and study teams
• Schedule patient visits and ensure protocol compliance
• Collect, verify, and maintain clinical data and source documentation
• Report adverse events and ensure regulatory compliance
• Prepare study reports and maintain accurate documentation for audits

Qualification
• M.Pharm (Master of Pharmacy) or B.Pharm (Bachelor of Pharmacy) from a recognized university

Experience
• Relevant experience in clinical research or clinical trial coordination preferred

Skills
• Knowledge of ICH-GCP guidelines and clinical trial processes
• Strong documentation and organizational skills
• Good communication and coordination abilities
• Attention to detail and compliance-focused approach
• Basic computer proficiency (MS Office applications)

No. of Vacancy: 01

Important Date
• Date of Walk-In: 23-02-2026

About the Organization
The Tata Memorial Centre (TMC) is a premier cancer treatment and research institution under the Department of Atomic Energy, Government of India, dedicated to advanced oncology care, research, and clinical trials.

Official Notification Click Here