Life Science Job at Tata Memorial Centre
Looking for Life Science Jobs in the clinical research sector? Here’s an excellent opportunity from Tata Memorial Centre Jobs for qualified Life Sciences, Biotechnology, Pharmacy, Zoology, and Botany postgraduates. The prestigious Homi Bhabha Cancer Hospital & Research Centre, Muzaffarpur, has announced a Trial Coordinator vacancy under a major oncology clinical research project. Candidates interested in clinical trials, cancer research, and healthcare innovation should not miss this opportunity to build a rewarding career in one of India’s leading cancer research institutions.
About Tata Memorial Centre Jobs
Tata Memorial Centre (TMC) is one of India’s most respected cancer treatment and research institutions operating under the Department of Atomic Energy, Government of India. Through its network of hospitals and research centres, TMC contributes significantly to cancer care, clinical trials, translational research, and healthcare innovation. Tata Memorial Centre Jobs are highly sought after by candidates looking to establish successful careers in oncology, biomedical sciences, and clinical research.
Job Details:
- Job Title: Trial Coordinator
- Organization: Tata Memorial Centre
- Project: BTCSELECT (TMC-TRAC Funded)
- Location: Muzaffarpur
- Employment Type: Project-Based Contract
- Project Account No.: 5824
- Advertisement No.: HBCH&RC/PROJECT/2026/P13
Role Overview
The Trial Coordinator will support the execution and management of the BTCSELECT clinical research project, a Phase III randomized clinical trial evaluating chemotherapy regimens for patients with locally advanced or metastatic biliary tract cancers. The role involves coordinating clinical research activities, maintaining study documentation, ensuring protocol compliance, and supporting trial operations.
Project Title
A Two-Arm Randomized Phase III, Open-Label, Prospective Non-Inferiority Study of Irinotecan versus Oxaliplatin/5-FU-Based Chemotherapy (mFOLFOX/CAPOX) for Patients with Locally Advanced/Metastatic Biliary Tract Cancers (BTC) Previously Treated with Gemcitabine-Cisplatin-Based Chemotherapy.
Vacancy Details
| Position | Vacancies | Monthly Remuneration |
|---|---|---|
| Trial Coordinator | 01 | ₹30,000 per month |
Educational Qualification
Candidates must possess:
- Postgraduate Degree in:
- Life Sciences
- Biotechnology
- Zoology
- Botany
- Other relevant Science disciplines
- AND
- PG Diploma in Clinical Research (Mandatory)
Experience
Desirable:
- Minimum one year of experience in clinical research, clinical trial coordination, or related research projects.
Age Limit
Maximum 35 years as on the date of interview.
Key Responsibilities
- Coordinate day-to-day clinical trial activities.
- Maintain study documentation and regulatory records.
- Assist investigators in patient recruitment and follow-up.
- Ensure protocol compliance and adherence to Good Clinical Practice (GCP) guidelines.
- Support data collection, verification, and reporting activities.
- Coordinate communication among investigators, sponsors, and research teams.
- Facilitate monitoring visits and audit readiness.
- Manage clinical trial documentation and participant records.
Contract Duration
- Initially for 6 months, or
- Till continuation/completion of the project, whichever is earlier.
Walk-In Interview Details
| Particulars | Details |
|---|---|
| Interview Date | 19 June 2026 (Friday) |
| Reporting Time | 9:00 AM – 10:00 AM |
| Mode | Walk-In Interview |
| Interview Venue | Homi Bhabha Cancer Hospital and Research Centre Shri Krishna Medical College and Hospital Campus Umanagar, Muzaffarpur, Bihar – 842004 |
Documents Required
Candidates should bring:
- Updated Bio-data / CV
- Recent Passport Size Photograph
- Original and self-attested copies of:
- Educational Certificates
- Experience Certificates
- PAN Card
- Aadhaar Card
- Relevant supporting documents
Preferred Candidate Profile
- Background in Life Sciences, Biotechnology, or related disciplines.
- Understanding of clinical research and trial management.
- Familiarity with clinical trial documentation and regulatory requirements.
- Strong organizational, communication, and documentation skills.
- Ability to work with investigators, patients, and multidisciplinary healthcare teams.
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