TMC Clinical Research Coordinator RARExCAN Recruitment 2026

TMC Clinical Research Coordinator Recruitment 2026: Overview

Tata Memorial Centre (TMC), a grant-in-aid institution under the Department of Atomic Energy, is hiring a Clinical Research Coordinator at Tata Memorial Hospital in Mumbai. This project appointment supports RARExCAN, a network focused on rare cancers and exceptional responders in India. The project aims to speed up translational research, and the notice identifies it through project account number 6354.

Service Conditions and Caveats

• Initial term: The appointment starts with a six-month engagement linked to the RARExCAN project. The notice does not promise an extension or a permanent appointment.
• Complete information: TMC can reject an incomplete form. Make sure your answers give a complete and accurate account of the information requested in the application.
• Accuracy throughout recruitment: Incorrect information, missing material facts or failure to meet the stated conditions can lead to cancellation. If TMC discovers such a problem after appointment, it may end your employment.
• Interview calls: Sending a form does not guarantee that TMC will call you. The centre retains the right to withhold an interview call without giving a reason.
• Travel arrangements: If you come from outside Mumbai, arrange your own stay. TMC will not provide accommodation.
• Email contact: Use a valid email address that you can access. TMC will send correspondence and interview information by email, so check your inbox and spam folder.
• Your follow-up: You are responsible for receiving, downloading and printing the material TMC sends you. The centre does not accept responsibility for missed messages caused by an incorrect email address or spam filtering.
• Application receipt: TMC does not take responsibility if your online application is not received.
• Questions about this notice: Contact 24177000, extension 4664, or email kevatncg.tmh@tmc.gov.in for clarification.

• Assist the principal investigator and co-investigator with screening trial participants.
• Record the informed consent process.
• Check that trial activities follow the study protocol.
• Handle communication with the Institutional Ethics Committee.
• Manage study data and keep the Investigator Study File updated.
• Process reimbursements for study participants.
• Keep study trackers and logs up to date.