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TMC-HBCHRC Recruitment: Trial Coordinator (Muzaffarpur)

Pharm'Up 2 min read

The Tata Memorial Centre (TMC), an autonomous body under the Department of Atomic Energy, is inviting applications for a Trial Coordinator position at the Homi Bhabha Cancer Hospital and Research Centre (HBCHRC) in Muzaffarpur, Bihar. This role is ideal for pharmacy and life science graduates looking to build a career in clinical trial management within a premier oncology research environment.


Position Details

  • Post Name: Trial Coordinator
  • Number of Vacancies: 01
  • Remuneration: ₹25,000 per month
  • Age Limit: Maximum 35 years (as of the walk-in date)
  • Tenure: Initially for six months or until the project concludes.

Eligibility Criteria

A PG Diploma in Clinical Research is mandatory for this role. Candidates must meet one of the following education tracks:

  • Option A: Postgraduate degree in Science (M.Pharm, Biotech, Zoology, Botany, Life Sciences, etc.) + PG Diploma in Clinical Research. (1 year of experience is desirable).
  • Option B: Graduate degree in Science + PG Diploma in Clinical Research + 1 year of experience is mandatory/desirable.

Interview & Application Process

TMC is offering both Physical Walk-In and Online Interview options for outstation candidates.

1. For Online Interview (Outstation Candidates)

  • Requirement: Send your resume and supporting documents in a single PDF file.
  • Email to: recruitment@hbchrcmzp.tmc.gov.in
  • Subject Line: Must clearly mention the post applied for.
  • Deadline for Email: April 10, 2026, by 3:00 PM.
  • Note: Only shortlisted candidates will be contacted for the online session.

2. For Physical Walk-In Interview

  • Date: Monday, April 13, 2026
  • Registration Time: 9:00 AM to 10:00 AM
  • Venue: Homi Bhabha Cancer Hospital and Research Centre, SKMCH Campus, Umanagar, Muzaffarpur, Bihar – 842004.

Role Responsibilities

Trial Coordinators at TMC generally oversee:

  • Patient recruitment and screening for clinical trials.
  • Maintaining Case Report Forms (CRFs) and regulatory documents.
  • Coordinating between investigators, ethics committees, and sponsors.
  • Ensuring compliance with ICH-GCP guidelines.

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