Clinical Research Coordinator

Roles & Responsibilities
• Coordinate day-to-day clinical trial activities as per study protocol
• Assist investigators in patient screening, enrollment, and follow-up
• Ensure informed consent process is completed and documented correctly
• Maintain study documents, source records, and trial master files
• Coordinate with investigators, nurses, sponsors, and CRO teams
• Support data collection, CRF completion, and query resolution
• Ensure compliance with ICH-GCP guidelines and institutional SOPs
• Assist during monitoring visits, audits, and inspections
• Track study timelines and report progress to the study team

Qualification
• B.sc, B.Pharm, or Post-Graduation in Life Sciences or related field

Experience
• Minimum One Year of Experience in Clinical Research Mandatory

Skills
• Good understanding of clinical research processes and GCP guidelines
• Strong documentation and organizational skills
• Effective communication and coordination abilities
• Attention to detail and ability to manage multiple tasks
• Proficiency in MS Word, Excel, and basic data handling

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

Walk-in Interview Details
• Date: 20-02-2026
• Venue: HRD Meeting Room, 3rd Floor, Main Building, Dr. E. Borges Marg, Parel, Tata Memorial Hospital, Mumbai – 400012

About the organization
Tata Memorial Hospital is one of India’s premier cancer care and research institutes, known for excellence in clinical research, patient care, and medical education, contributing significantly to advancing oncology research and treatment.

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