MSD Hiring Clinical Trial Coordinator in Gurgaon
MSD (Merck & Co.) is hiring for the role of Clinical Trial Coordinator at its Gurgaon location. This opportunity is ideal for candidates with a life sciences background and 0 to 3 years of clinical research experience. The role involves supporting clinical trial operations, site administration, regulatory coordination, document management, and financial tracking, making it a strong entry point into global clinical research.
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🏢 Company Details
MSD (Merck & Co.) is a leading global biopharmaceutical company focused on delivering innovative medicines and vaccines. The company operates under strict ICH‑GCP standards and global clinical trial frameworks, providing employees with exposure to high‑quality research, regulatory systems, and multinational study environments.
📊 Job Role Overview
- Company Name: MSD (Merck & Co.)
- Job Role: Clinical Trial Coordinator
- Employment Type: Full‑Time
- Experience Required: 0–3 Years
- Functional Area: Clinical Operations / Trial Management
- Job Location: Gurgaon
- Educational Qualification: Life Sciences degree
📋 Job Responsibilities
- Tracking essential documents and study materials
- Managing safety report distribution and tracking
- Updating clinical trial databases (e.g., CTMS) and trackers
- Supporting clinical and non‑clinical supply management
- Coordinating labeling and translation activities
- Supporting site start‑up documentation and submissions
- Coordinating with investigators for required regulatory forms
- Tracking and managing insurance certificates and approvals
- Assisting with submissions for IRB/ERC and regulatory authorities
- Supporting publishing of study results as per local guidelines
🎓 Qualification Required
Candidates applying for this role should meet the following requirements:
- Educational Qualification:
- B.Pharm / M.Pharm (Life Sciences background preferred)
- Bachelor’s degree in Life Sciences or healthcare‑related field
- Experience Requirement:
- 0–3 years of experience in:
- Clinical research
- clinical operation
- Clinical trials
🧠 Required Skills
- Good understanding of:
- Clinical trials lifecycle
- Clinical trial documentation
- CTMS and eTMF systems
- Basic knowledge of:
- ICH‑GCP guidelines
- Regulatory processes
- Strong analytical and problem‑solving abilities
- Organizational and multitasking skills
- Attention to detail and documentation accuracy
⭐ Job Summary
The Clinical Trial Coordinator role at MSD is a comprehensive entry‑level clinical operations role that covers multiple aspects of trial execution—from documentation and regulatory tasks to budgeting and site coordination. This makes it an excellent gateway to advanced roles like CRA, Clinical Project Management, or Regulatory Affairs, especially for candidates aiming for global pharma careers.
🎯 Suitable Candidates
- Life sciences graduates
- Freshers or candidates with 0–3 years of experience
- Individuals interested in clinical operations and trial management
- Candidates aiming for long‑term careers in CRAs, CTAs, or PM roles
🏢 Work Environment
- Occasional travel based on project requirements
- Remote work setup with global collaboration
- Exposure to international project teams
- Structured workflow aligned with regulatory compliance standards
💡 Expert Tips
- Highlight attention to detail and analytical ability in your resume
- Revise medical terminology and coding concepts
- Learn basics of clinical trials and CDM processes
- Practice data accuracy and validation skills
- Avoid common pharma interview mistake
💰 Compensation Insight
- Entry-level roles typically offer competitive salaries as per industry standards
- Salary depends on experience, skills, and company policies
- Growth opportunities in terms of salary and roles are strong in this field
- Even if you start at an entry level, your career can grow quickly with the right experience.
🌟 Why Join MSD?
Here are some reasons why this opportunity is valuable:
- ✅ Work with a globally recognized pharmaceutical company
- ✅ Gain exposure to international clinical trial standards
- ✅ Learn real-time clinical research processes
- ✅ Opportunity to work with experienced professionals
- ✅ Strong career growth opportunities
🔗 How to apply
Interested candidates should apply only through the official company career website using the link provided below.
Important Disclaimer: This job post is shared for informational purposes only, based on publicly available job details. Candidates are advised to verify eligibility, job responsibilities, and application procedures from the official website before applying.
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📚 Career Guide
- Common Mistake during interview and how to avoid them
- Best career option after b.pharm
- Clinical research roadmap
❓FAQ
1.What is CTMS and eTMF?
CTMS: A system to track clinical trial progress
eTMF: Digital storage of trial documents
2.How can I increase my chances of selection?
Learn basics of clinical trials
Add relevant keywords in your resume
Practice interview questions
Get referrals if possible
