🌍 MSD Hiring Sr Clinical Trial Coordinator | Global Clinical Trial Operations
🏢 About MSD (Merck & Co.)
MSD (Merck Sharp & Dohme) is a global healthcare leader dedicated to discovering, developing, and delivering innovative medicines and vaccines.
Through its Global Clinical Trial Operations (GCTO) division, MSD manages complex multinational clinical trials ensuring regulatory compliance, data integrity, and patient safety.
The company operates in over 140 countries and is known for maintaining the highest standards in clinical research and regulatory excellence.
📌 Job Overview
Position: Sr Clinical Trial Coordinator
Location: Gurugram, Haryana, India
Experience: 3–5 Years
Department: Global Clinical Trial Operations (GCTO)
Requisition ID: R384567
Application Deadline: 04 March 2026
🧾 Trial & Site Administration
- Track essential documents and safety reports
- Maintain CTMS and clinical databases
- Manage clinical & non-clinical supply logistics
- Coordinate labeling & translation change requests
- Ensure site readiness and activation timelines
📂 Clinical Documentation & eTMF Management
- Prepare, distribute, and archive study documents
- Execute eTMF Quality Control Plan
- Perform eTMF reconciliation & compliance checks
- Prepare Investigator Trial File (ITF) binders
- Ensure Good Documentation Practices (GDP)
📑 Regulatory & Site Start-Up Support
- Support IRB/ERC submission packages
- Coordinate regulatory authority submissions
- Track study insurance documentation
- Support study result publication compliance
💰 Budgeting, Contracts & Payments
- Develop & manage site budgets
- Negotiate Clinical Trial Agreements (CTRA)
- Manage contract lifecycle & amendments
- Process investigator grants & payments
- Ensure FCPA compliance documentation
⭐ Quality Oversight & Leadership
- Act as Subject Matter Expert (SME)
- Mentor junior coordinators
- Drive process improvement initiatives
- Support investigator meetings & study coordination
🎓 Qualifications & Skills
- Bachelor’s degree in Healthcare / Clinical Research / Administration
- 3–5 years clinical research experience
- Knowledge of ICH-GCP & clinical trial compliance
- Experience with CTMS & clinical IT systems
- eTMF & clinical documentation expertise
- Clinical Trial Agreements (CTA/CTRA) knowledge
- Budget negotiation & contract management skills
- Strong communication & multi-tasking ability
💰 Estimated Salary
₹10 – ₹16 LPA (Based on senior clinical trial coordinator roles in multinational pharma & CRO companies)
🌟 Why Join MSD?
- Global exposure in clinical trial operations
- Work in a multicultural matrix environment
- Strong training & mentorship programs
- Career progression within GCTO
- Industry-leading compliance standards
This is a senior-level clinical trial coordination role. Ensure your experience in CTMS, eTMF, regulatory submissions, and clinical trial agreements aligns with the job requirements before applying.
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