MSD Careers has announced a new opportunity for the role of Clinical Trial Coordinator under its Global Clinical Trial Operations team. This Clinical Trial Coordinator job is ideal for candidates with experience or interest in clinical trial management, site administration, regulatory documentation, and clinical operations.
The Clinical Trial Coordinator role at MSD involves managing trial documentation, supporting site start-up activities, maintaining CTMS and eTMF systems, coordinating regulatory submissions, and collaborating with CRAs, clinical operations managers, and finance teams.
Candidates searching for clinical trial coordinator jobs, clinical research jobs in pharma, clinical operations vacancies, or CTC jobs in India can consider this opportunity from MSD.
Job Details
| Particulars | Details |
|---|---|
| Job Role | Clinical Trial Coordinator |
| Company | MSD |
| Employment Type | Full-Time |
| Department | Clinical Operations |
| Requisition ID | R398335 |
| Job Posting End Date | 21 May 2026 |
| Work Arrangement | Not Applicable |
| Experience | Freshers & Experienced |
| Industry | Clinical Research / Pharmaceutical |
Key Responsibilities of Clinical Trial Coordinator
The Clinical Trial Coordinator at MSD will support end-to-end clinical trial activities, including:
Trial & Site Administration
- Track essential clinical trial documents and safety reports
- Maintain CTMS trackers and reporting tools
- Support clinical and non-clinical supply management
- Coordinate labeling and translation requests
Document Management
- Prepare, collate, archive, and distribute clinical documents
- Support eTMF reconciliation and quality control
- Prepare investigator trial binders
- Coordinate translations and document destruction processes
Regulatory & Site Start-Up Activities
- Support IRB/ERC submission packages
- Track study insurance certificates
- Assist with regulatory authority submissions
- Coordinate site evaluation and validation documentation
Budgeting & Payment Coordination
- Assist with site budgets and CTRAs
- Track contract negotiations
- Coordinate investigator and vendor payments
- Ensure compliance with financial procedures
Meeting & Study Coordination
- Organize investigator meetings
- Prepare study memos and protocol-related materials
- Coordinate vendors and study logistics
Required Skills
MSD is looking for candidates with skills in:
- Clinical Trial Management
- Clinical Trial Documentation
- CTMS & eTMF Management
- ICH-GCP Guidelines
- Regulatory Affairs
- Clinical Operations
- Budget Management
- Supply Management
- Data Analysis
- Site Management
- Clinical Trial Compliance
Educational Qualification
Candidates from the following backgrounds may be eligible:
- B.Pharm
- M.Pharm
- Pharm.D
- BSc Life Sciences
- MSc Life Sciences
- Biotechnology
- Clinical Research
- Related Healthcare Disciplines
Why Join MSD?
Working at MSD offers exposure to global clinical trials, international regulatory processes, and advanced clinical operations systems. Employees gain opportunities to work with cross-functional global teams while contributing to innovative healthcare research.
Benefits May Include:
- Global work environment
- Career growth in clinical research
- Exposure to international clinical studies
- Learning opportunities in regulatory and trial management
- Diverse and inclusive workplace culture
How to Apply
