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Clinical Trial Coordinator Job at MSD | 0 – 3 Years
🏢 MSD
📍 Gurgaon
🧪 Clinical Operations
📂 CTMS & eTMF
🎓 0–3 Years
MSD is hiring Clinical Trial Coordinators under its Global Clinical Trial Operations team for candidates interested in clinical trial management, regulatory documentation, CTMS, and site administration.
This opportunity is ideal for candidates looking to build careers in Clinical Research, Clinical Operations, Trial Coordination, Regulatory Affairs, and Clinical Trial Management.
📋 Job Overview
- Company: MSD
- Job Role: Clinical Trial Coordinator
- Department: Clinical Operations
- Location: Gurgaon, Haryana
- Employment Type: Full-Time
- Experience: Freshers & Experienced
- Industry: Clinical Research / Pharmaceutical
- Requisition ID: R398335
- Last Date to Apply: 21 May 2026
💰 Estimated Salary: ₹4.5 – ₹8.5 LPA
📌 Key Responsibilities
🧪 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 and archive clinical trial documents
- Support eTMF reconciliation and quality checks
- Prepare investigator trial binders
- Coordinate translations and document processes
📑 Regulatory & Site Start-Up Activities
- Support IRB/ERC submission packages
- Track study insurance certificates
- Assist regulatory authority submissions
- Coordinate site validation documentation
💰 Budgeting & Study Coordination
- Support site budgets and CTRAs
- Coordinate investigator and vendor payments
- Organize investigator meetings
- Support study logistics and reporting
📚 Clinical Research Resources
👉 Clinical Research Coordinator Guide
👉 Clinical Trial Assistant Quiz
👉 CDISC SDTM & ADaM Guide
👉 Explore Knowledge Hub
🎓 Eligibility Criteria
📚 Educational Qualification
- B.Pharm
- M.Pharm
- Pharm.D
- BSc / MSc Life Sciences
- Biotechnology
- Clinical Research
- Related Healthcare Disciplines
💡 Required Skills
- Clinical Trial Management
- CTMS & eTMF Management
- ICH-GCP Guidelines
- Regulatory documentation
- Clinical operations coordination
- Budget and vendor management
- Communication and teamwork skills
🌍 Why Join MSD?
- Exposure to global clinical trials
- Career growth in clinical operations
- Hands-on experience in CTMS and eTMF systems
- Learning opportunities in regulatory affairs
- International work environment
- Cross-functional collaboration with global teams
📈 Career Growth Resources
👉 Best Career Options After B.Pharm
👉 Pharmacovigilance Salary Guide
👉 Healthcare IT vs Clinical Healthcare
📄 Resume Tips
- Highlight clinical research internships or projects
- Mention CTMS, eTMF, or GCP knowledge
- Add certifications related to Clinical Research
- Use ATS-friendly formatting
- Showcase coordination and documentation skills
- Keep resume concise and professional
🎯 Interview & Preparation Resources
👉 Resume & Career Growth Guide
👉 Aptitude & Reasoning Quiz
👉 Explore More Healthcare Quizzes
🧩 Fun Learning & Career Growth
Improve your healthcare and clinical research knowledge with quizzes and puzzles.
🚀 Job Application Link
📌 Important Note Before You Apply:
Please make sure to read the complete job description carefully before submitting your application. Make sure your clinical research interests and qualifications align with the role requirements before proceeding.
Please make sure to read the complete job description carefully before submitting your application. Make sure your clinical research interests and qualifications align with the role requirements before proceeding.
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