ACTREC Trial Co-Ordinator Walk-In Interview 2026

ACTREC's Centre for Cancer Epidemiology (CCE) is hiring 1 Trial Co-Ordinator on a project basis in Navi Mumbai. If you have a B.Sc with a PG Diploma in Clinical Research, you can walk in for an interview on 27 July 2026. The pay is Rs. 30,000 per month. The post is initially for 6 months or until the project ends, whichever comes first.

Advanced Centre for Treatment, Research and Education in Cancer (ACTREC) Trial Co-Ordinator Walk-In Interview 2026

The Centre for Cancer Epidemiology (CCE), a unit of ACTREC under the Tata Memorial Centre, has released a walk-in interview notice (Advt No. CCE/Advt/228/2026) for the post of Trial Co-Ordinator to support an ongoing clinical research project. No online application is required — you just need to walk in with your documents on the interview date. Candidates with an M.Sc in Clinical Research will have an edge.

Who Can Apply?

• Qualification: B.Sc with a PG Diploma in Clinical Research (mandatory).
• Preferred: M.Sc in Clinical Research is desirable.

Salary

• You will get a pay of Rs. 30,000 per month for this project position.

Selection Process (Walk-In Interview)

ACTREC's Centre for Cancer Epidemiology will select candidates directly through a walk-in interview:

1. Document Verification: Bring your bio-data, original certificates, qualification certificates, experience certificates, birth certificate, photo, and PAN Card, along with a set of Xerox copies.
2. Interview: Eligible candidates will be interviewed on the spot at the venue.

How to Apply

1. Prepare your bio-data, original certificates, qualification certificates, experience certificates, birth certificate, photo, and PAN Card, with a set of Xerox copies.
2. Reach Room No. 205, 2nd Floor, Centre for Cancer Epidemiology, ACTREC, Sector 22, Kharghar, Navi Mumbai - 410210 between 9:00 AM and 10:00 AM on the interview date.
3. Attend the walk-in interview along with your original documents for verification.

Important Dates

• Notification Date: 20 July 2026
• Walk-In Interview Date: 27 July 2026 (Monday)

• Coordinate day-to-day activities of clinical trials at the Centre
• Maintain trial documentation, case report forms, and patient records
• Schedule patient visits and track trial timelines
• Ensure trials follow Good Clinical Practice (GCP) guidelines
• Liaise with investigators, sponsors, and ethics committees
• Monitor patient enrollment, consent, and follow-up procedures
• Prepare progress reports for ongoing clinical research studies