Clinical Trial Coordinator Jobs at MSD for Pharma Graduates | Apply Online
An MSD Clinical Trial Coordinator opportunity has emerged for aspiring professionals in the pharmaceutical field. MSD is inviting applications from qualified candidates interested in a rewarding career in clinical research. This position is based in Gurgaon, Haryana, and has a deadline for applications on 26 August 2026.
Job Details
- Job Title: Clinical Trial Coordinator
- Location: Gurgaon, Haryana (Vatika Towers)
- Job Type: Full-time
- Posted On: Today
- End Date to Apply: 26 August 2026
- Job Requisition ID: R411062
About the Company
MSD, known as Merck & Co., Inc., is a global healthcare leader that operates in the pharmaceutical sector. The organization is dedicated to improving health outcomes through innovative medicines, vaccines, and animal health products. With a commitment to research and development, MSD plays a pivotal role in advancing healthcare solutions worldwide. The clinical trial coordinator jobs at MSD are critical for ensuring the smooth operation of clinical studies and maintaining compliance with regulatory standards.
MSD Clinical Trial Coordinator Job Description
The MSD Clinical Trial Coordinator (CTC) plays a vital role under the guidance of the line manager. This position is responsible for comprehensive trial and site administration, which includes preparing, collating, distributing, and archiving clinical documents. The CTC will support clinical supply and non-clinical supply management while ensuring timely maintenance of tracking and reporting tools. This role is essential for meeting planned Site Ready dates and involves collaboration with various stakeholders, including finance representatives for managing CTRAs and payments.
Key Responsibilities
- Trial and Site Administration:
- Track essential documents and report safety reports.
- Ensure collation and distribution of study tools and documents.
- Update clinical trial databases (CTMS) and trackers.
- Manage clinical and non-clinical supply in collaboration with other country roles.
- Coordinate labeling requirements and translation change requests.
- Document Management:
- Prepare documents and correspondence.
- Collate, distribute, and archive clinical documents, including eTMF.
- Assist with eTMF reconciliation and execute the eTMF Quality Control Plan.
- Update manuals and documents, including patient diaries.
- Document the proper destruction of clinical supplies.
- Regulatory & Site Start-Up Responsibilities:
- Provide and collect forms for site evaluation and submissions in a timely manner.
- Obtain, track, and update study insurance certificates.
- Support the preparation of submission packages for IRB/ERC and regulatory agencies.
- Publish study results as required by local legislation.
- Budgeting, Agreement, and Payments:
- Collaborate with finance representatives to manage budgets and contracts.
- Track and report contract negotiations.
- Calculate and execute payments to investigators and vendors.
- Ensure adherence to financial and compliance procedures.
- Meeting Planning:
- Organize meetings and support local investigator meetings.
Clinical Trial Coordinator Skills
- Adaptability
- Clinical Research
- Clinical Site Management
- Clinical Trial Management
- Regulatory Affairs Compliance
- Patient Recruitment
Why Join as an MSD Clinical Trial Coordinator?
Joining MSD as a Clinical Trial Coordinator offers an opportunity to be part of a leading global healthcare organization committed to innovation and excellence in clinical research. The organization fosters a collaborative environment where professionals can grow and contribute to meaningful health solutions. With a focus on employee development and adherence to the highest standards of compliance, MSD provides a supportive workplace for its employees.
Conclusion
The clinical trial coordinator jobs at MSD present a significant opportunity for pharma graduates eager to advance their careers in clinical research. With a focus on collaboration and compliance, this role is crucial for the successful execution of clinical trials. Interested candidates are encouraged to apply before the deadline of 26 August 2026 to secure their chance to be part of this esteemed organization.
