ACTREC Sr Research Fellow Recruitment 2026

About This Job

ACTREC is hiring a Senior Research Fellow (SRF) for the Institutional Ethics Committee-III of the Institutional Research Board at Tata Memorial Centre. If you have a postgraduate degree in Science, a PG Diploma in Clinical Research, and at least 3 years of clinical trial monitoring experience, you can attend the walk-in interview. The interview is on 13 May 2026, and reporting time is 10:00 a.m. to 10:30 a.m.. Salary ranges from Rs. 28,450 to Rs. 60,000 per month based on experience.

ACTREC Senior Research Fellow Recruitment 2026

The Advanced Centre for Treatment Research and Education in Cancer (ACTREC), Tata Memorial Centre, has released advertisement OS-A/57/2026 dated 4 May 2026 for a Senior Research Fellow role at Kharghar, Navi Mumbai. The position is on an outsourced contract basis through A-1 Facility and Property Managers Pvt. Ltd. This is a clinical research monitoring role linked to Institutional Ethics Committee-III, so it is best suited for people who already handle interventional clinical trials.

The selected person will be placed at TMC-ACTREC, Kharghar, Navi Mumbai 410210. The initial duration is 6 months. The work profile is focused on monitoring research studies at Tata Memorial Centre, especially studies reviewed through the Institutional Ethics Committee and Institutional Research Board system.

The notice makes this a specialized clinical research role, not a fresher research post. Your experience should cover monitoring or handling interventional clinical trials, including randomized controlled trials. Oncology exposure is preferred because ACTREC and Tata Memorial Centre work in a cancer treatment and research environment. The salary range also depends on experience above the minimum eligibility, so keep clear proof of your clinical trial monitoring work ready for the interview.

Who Can Apply?

Educational Qualification

• Qualification: You need post graduation in Science such as M. Pharma, Life Science, Biotech, Zoology, or Botany.
• Clinical Research: You must also have a PG Diploma in Clinical Research.
• Experience: You need 3 or more years of experience in monitoring or handling interventional clinical trials, including RCTs.
• Preferred Area: Experience in oncology clinical trials is preferred.
• Study Type: The notice highlights experience with interventional clinical trials and RCT handling.

Other Requirements

• Work Area: The role supports Institutional Ethics Committee-III and research-study monitoring at TMC.
• Interview Mode: You must attend the walk-in interview physically at ACTREC, Kharghar.
• Contract Basis: The engagement is for 6 months on outsourced contract terms.

Age Limit

• Maximum age: 35 years.
• Relaxation: The notice says age may be relaxed based on experience.
• Reference Date: A separate age reference date is not mentioned in the notification.

Salary

• Consolidated monthly salary: Rs. 28,450 to Rs. 60,000 per month.
• The exact amount will depend on experience above the specified eligibility criteria.
• Duration of engagement: 6 months.
• Separate allowances are not mentioned in the notification.

Application Fee

• The notification does not mention any application fee.
• You need to attend the walk-in interview with the listed documents.

Selection Process (No Written Exam)

Selection will be through a walk-in interview after document checking at ACTREC. The notification does not mention any written exam or online test for this Senior Research Fellow role.

1. Reporting: Reach the venue between 10:00 a.m. and 10:30 a.m. on 13 May 2026.
2. Document Verification: ACTREC will check your bio-data, ID proof, qualification documents, and experience certificates.
3. Interview: The panel will assess your clinical research background, trial monitoring experience, and fit for IEC-III research-study monitoring.
4. Experience Review: Your 3+ years of RCT or clinical trial monitoring experience may be checked through certificates and bio-data details.

How to Apply

1. Prepare your bio-data with education, clinical research diploma details, and trial-monitoring experience.
2. Keep a recent passport-size photograph, Aadhaar Card copy, and PAN Card copy ready.
3. Carry original certificates and self-attested copies of qualification and experience certificates.
4. Keep proof of clinical research diploma and trial-monitoring experience easy to find during document checking.
5. Go to 3rd Floor, PS-306, Paymaster Shodhika, TMC-ACTREC, Sector 22, Kharghar, Navi Mumbai 410210.
6. Report between 10:00 a.m. and 10:30 a.m. on Wednesday, 13 May 2026.

Documents to Carry

• Bio-data with education, clinical research training, and work experience details.
• Recent passport-size photograph.
• Aadhaar Card and PAN Card copies, as mentioned in the notification.
• Original qualification certificates and self-attested copies.
• Original experience certificates and self-attested copies showing 3+ years of trial-monitoring work.
• Clinical Research PG Diploma proof because it is an essential requirement for this SRF role.
• RCT or interventional trial proof, such as appointment letters, experience letters, or project certificates, if available.
• Oncology trial experience proof, if you have it, because the notice says oncology experience is preferred.

Important Dates

• Notification Date: 4 May 2026
• Walk-In Interview Date: 13 May 2026
• Reporting Time: 10:00 a.m. to 10:30 a.m.
• Initial Contract Duration: 6 months
• Interview Venue: 3rd Floor, PS-306, Paymaster Shodhika, TMC-ACTREC, Sector 22, Kharghar, Navi Mumbai 410210

• Monitor research studies handled through Institutional Ethics Committee-III
• Review clinical trial documentation and follow study-monitoring processes
• Coordinate with TMC research teams for interventional clinical trial follow-up
• Keep clear records of monitoring observations, study status, and pending actions
• Assist the Institutional Research Board with ethics committee documentation work
• Follow clinical research, confidentiality, and institutional compliance rules
• Prepare updates for supervisors on study monitoring and trial handling activities