TMC Clinical Trial Assistant Walk-in Interview 2026

Tata Memorial Centre (TMC) is hiring a Clinical Trial Assistant for its National Cancer Grid Project at Tata Memorial Hospital, Mumbai. If you have a B.Sc/M.Sc in Life Science or B.Pharm/M.Pharm with a diploma or master's degree in Clinical Research, you can walk in for the interview on 21 August 2026. This is a project post initially for six months, with a starting salary between Rs. 40,000 and Rs. 43,000 per month. The age limit is 35 years.

Tata Memorial Centre (TMC) Clinical Trial Assistant Walk-in Interview 2026

Tata Memorial Centre (TMC), a Grant-in-Aid Institution under the Department of Atomic Energy, Government of India, has announced a walk-in interview for the post of Clinical Trial Assistant under the "National Cancer Grid" Project (Account No. 5377) at Tata Memorial Hospital, Parel, Mumbai. The National Cancer Grid links cancer centres across India for cancer care, research, and training, and this position supports the monitoring and documentation of clinical trials conducted under it. As a Clinical Trial Assistant, you will act as the in-house support resource for the monitoring team — helping with study start-up work, maintaining trial documentation, and coordinating monitoring visits alongside Clinical Research Associates (CRAs), Clinical Team Leads, the Project Manager, and the Finance Officer. There is no online application for this post — you need to attend the walk-in interview in person with your documents.

Who Can Apply?

For Rs. 40,000/month:

• You need a B.Sc or M.Sc in Life Science, or a B.Pharm/M.Pharm, along with a Post Graduate Diploma in Clinical Research (PGDCR) or an M.Sc. in Clinical Research.

For Rs. 43,000/month:

• You need the same base qualification (B.Sc/M.Sc in Life Science or B.Pharm/M.Pharm) along with an M.Sc. in Clinical Research and at least one year of relevant experience.

• Desirable: Experience handling global and multi-centric clinical trials is an advantage.
• Desirable: Good verbal and written communication skills, and fluency in English.
• A diploma or degree specifically in Clinical Research is preferred over a general Life Science background.
• If you already work at TMC, you must bring a No Objection Certificate (NOC) from your current Head of Department or Principal Investigator.

Age Limit

• You should be up to 35 years old to apply for this post.

Salary

• If you have a PGDCR or M.Sc. Clinical Research without prior experience, your starting pay will be Rs. 40,000 per month.
• If you have M.Sc. Clinical Research with one year of experience, your starting pay will be Rs. 43,000 per month.
• This is a fixed, consolidated monthly remuneration for the six-month project post — no separate allowances are mentioned in the notification.

Selection Process

Since this is a walk-in interview, the process is simpler and faster than a typical exam-based recruitment:

1. Document Verification: When you arrive, your bio-data, photograph, and original certificates will be checked against the attested copies you bring.
2. MCQ Test (conditional): If a large number of candidates turn up, TMC will hold a short MCQ test on the spot to shortlist candidates for the interview.
3. Walk-in Interview: Shortlisted candidates will be interviewed the same day by the selection panel.

How to Apply

1. There is no online application for this post — you must attend in person.
2. Reach IRB Meeting Room, 3rd Floor, Main Building, Dr. E. Borges Marg, Parel, Tata Memorial Hospital, Mumbai – 400012 between 9:30 AM and 10:00 AM on 21 August 2026.
3. Carry your bio-data, a recent passport-size photograph, a photocopy of your PAN card, a photocopy of your Aadhaar card, and your original certificates along with a set of attested copies.
4. If you currently work at TMC, bring an NOC from your HOD or Principal Investigator.

Important Dates

• Notification Date: 14 August 2026
• Walk-in Interview Date: 21 August 2026
• Reporting Time: 9:30 AM to 10:00 AM

• Support all study start-up activities for the clinical trial monitoring group
• Maintain and organize documentation for ongoing clinical trials
• Assist Clinical Research Associates (CRAs) during monitoring visits, including travel coordination
• Coordinate closely with Clinical Team Leads, the Project Manager, and the Finance Officer
• Track compliance with applicable clinical research guidelines, rules, and regulations
• Prepare and update trial-related records and files for audits
• Communicate with the study team to ensure smooth day-to-day trial operations