Clinical Research Coordinator

Roles & Responsibilities
• Coordinate day-to-day activities of Phase II oncology clinical trials
• Assist investigators in protocol implementation and study documentation
• Maintain Clinical Trial Files (CTF), CRFs, and essential regulatory documents
• Ensure compliance with ICH-GCP, ethics committee, and sponsor requirements
• Support patient recruitment, informed consent process, and follow-up visits
• Manage data collection, query resolution, and study tracking activities
• Liaise with clinical teams, study monitors, and regulatory authorities
• Support multicentric and investigator-initiated oncology trials

Qualification
• B.Sc / B.Pharm / Graduate in Life Sciences
• PG Diploma in Clinical Research – Mandatory

Experience
• Minimum 1 year of clinical research experience
• Oncology trial exposure preferred

Age Limit
• Up to 35 years

No. of Post: 02

Skills
• Knowledge of ICH-GCP and clinical trial regulations
• Strong documentation and regulatory file management skills
• Good coordination and communication abilities
• Attention to detail and compliance orientation
• Ability to manage patient scheduling and trial timelines

Walk-In Interview Details
(As per official notification by Tata Memorial Hospital – candidates are advised to refer to the official advertisement for date, time, and venue details.)

About the Organization
Tata Memorial Hospital (TMC) is a premier cancer treatment and research institute under the Department of Atomic Energy, Government of India, known for its leadership in oncology care, clinical research, and advanced cancer therapies across India.

OFFICIAL NOTICE CLICK HERE