MSD (Merck Sharp & Dohme) has announced an opening for the position of Specialist, Clinical Research Associate at its Gurgaon location in Haryana. This is a full-time, regular employment opportunity based at the company’s Vatika Towers location.
The role focuses on clinical trial site management, monitoring, study compliance and maintaining strong relationships with investigators and site teams. The selected professional will work under the guidance of the CRA Manager and support assigned clinical research protocols and sites in accordance with applicable clinical research standards and regulations.
The application deadline for this position is October 14, 2026. Candidates interested in clinical research and clinical trial monitoring can apply through the official MSD careers portal.
MSD Recruitment 2026 – Job Highlights
| Particular | Details |
|---|---|
| Company | MSD (Merck Sharp & Dohme) |
| Job Title | Specialist, Clinical Research Associate |
| Job Function | Clinical Research / Clinical Trials |
| Job Location | Gurgaon, Haryana |
| Office Location | Vatika Towers |
| Job Type | Full Time |
| Employee Status | Regular |
| Work Arrangement | Not Applicable |
| Requisition ID | R419942 |
| Posted | October 7, 2026 |
| Application Deadline | October 14, 2026 |
| Salary / CTC | Not specified |
About MSD
MSD, also known as Merck Sharp & Dohme, is a global healthcare and pharmaceutical organization involved in medicines, vaccines and clinical research. Its clinical development operations support the planning and execution of clinical studies while maintaining applicable quality and compliance standards.
Job Description
As a Specialist, Clinical Research Associate, the professional will be responsible for the performance and compliance of assigned clinical trial protocols and research sites within the country.
Working under the oversight of a CRA Manager, the role involves monitoring study activities, maintaining site relationships, reviewing regulatory documentation and ensuring that clinical research activities follow the applicable protocol, ICH-GCP requirements, local regulations and company procedures.
The position also includes supporting site development and contributing expertise to monitoring processes and systems.
Key Responsibilities
- Act as the primary contact for assigned clinical research sites throughout the study lifecycle.
- Build and maintain effective working relationships with investigators and site personnel.
- Conduct site management and monitoring activities according to the study protocol and applicable procedures.
- Develop a detailed understanding of assigned study protocols and related requirements.
- Support site readiness activities in coordination with other clinical research functions.
- Provide input during site identification, selection and validation activities.
- Perform remote and on-site monitoring activities.
- Review site-generated data to ensure completeness, accuracy and reliability.
- Help protect clinical study participants’ rights, safety and well-being.
- Conduct site visits, including validation, initiation, monitoring and close-out visits.
- Prepare timely and accurate visit and non-visit contact reports.
- Collect and review essential regulatory documents during study start-up, maintenance and close-out.
- Communicate with investigators and site teams regarding recruitment, retention, protocol deviations and regulatory documentation.
- Support sites during audits and inspections when required.
- Identify and address site performance, quality and compliance concerns.
- Escalate significant issues through the defined CRA escalation process.
- Coordinate with clinical operations, finance, regulatory affairs, pharmacovigilance, legal and other internal functions.
- Work with external vendors, ethics committees and regulatory authorities where required.
- Maintain clinical trial information and documentation in CTMS, eTMF and other relevant systems.
- Participate in co-monitoring visits when appropriate.
- Support knowledge sharing within the CRA team.
- Act as a process subject matter expert, buddy or mentor when required.
- Contribute to the identification and development of potential new clinical research sites.
- Help strengthen the clinical research capabilities of newly identified sites.
Required Skills and Competencies
The vacancy lists skills and knowledge areas including:
- Clinical research
- Clinical site management
- Clinical study management
- Clinical trial monitoring
- Clinical trial planning
- Clinical development
- Good Clinical Practice (GCP)
- Clinical data management principles
- Protocol adherence
- Protocol review
- Data monitoring and reporting
- Clinical reporting
- Document management
- Electronic Trial Master File (eTMF)
- On-site management
- Adverse event reporting
- Data analysis
- Accountability
- Adaptability
- Meeting facilitation
- Electronic clinical trial documentation and systems
Clinical Trial Monitoring Responsibilities
A major part of this position involves monitoring clinical trial sites. The CRA will be expected to assess site performance, review study data and documentation, communicate with site personnel and ensure that trial activities are conducted according to the protocol and applicable requirements.
The role can involve different types of site visits, including:
- Site validation visits
- Site initiation visits
- Routine monitoring visits
- Close-out visits
- Co-monitoring visits, where applicable
Regulatory and Compliance Responsibilities
The position requires close attention to clinical research compliance. Activities are expected to follow:
- ICH-GCP requirements
- Applicable country laws and regulations
- Study protocols
- Sponsor standard operating procedures
- Site Monitoring Plans
- Relevant quality standards
- Adverse event reporting requirements
The CRA will also support the identification and resolution of quality or compliance issues and assist with audits or inspections when required.
Systems and Documentation
The Specialist CRA will be responsible for maintaining appropriate study information and documentation in systems such as:
- Clinical Trial Management Systems (CTMS)
- Electronic Trial Master File (eTMF)
- Other clinical research and monitoring systems used for assigned studies
Accurate and timely documentation is an important part of the role.
Work Location and Work Arrangement
The position is based at:
Gurgaon, Haryana – Vatika Towers
The job listing identifies the position as full time and states that the remote type is Not Applicable. The listing does not specify a remote or hybrid arrangement.
Salary / CTC
MSD has not specified the salary or CTC for this position in the provided job posting. Candidates can refer to the official recruitment communication for compensation and other employment terms.
Career Scope
This position offers responsibilities across clinical trial monitoring, site management, regulatory documentation, clinical operations and compliance. The role also provides opportunities to contribute as a process subject matter expert and support knowledge sharing within the CRA team.
How to Apply for MSD Recruitment 2026
Eligible candidates can submit their application through the official MSD careers portal.
The job posting is scheduled to close on October 14, 2026. MSD states that applications should be submitted no later than the day before the listed closing date because the posting is effective until 11:59 PM on the day before the stated end date.
Important Details Before Applying
- The position is for a Specialist, Clinical Research Associate.
- The job location is Gurgaon, Haryana.
- The position is full time and regular.
- The role focuses on clinical trial site management and monitoring.
- Knowledge of GCP, clinical research and protocol compliance is important.
- The position involves interaction with investigators, site teams and multiple internal functions.
- On-site and remote monitoring activities may be part of the role.
- Salary information has not been provided.
- The application deadline listed by MSD is October 14, 2026.
- Candidates should review the official job posting carefully before submitting their application.
Frequently Asked Questions
1. What is the job title at MSD?
The position is Specialist, Clinical Research Associate.
2. Where is this MSD job located?
The position is based in Gurgaon, Haryana, at Vatika Towers.
3. Is this a full-time job?
Yes. The position is listed as Full Time with regular employee status.
4. What does the Specialist CRA role involve?
The role involves clinical trial site management, monitoring, regulatory documentation, compliance, investigator communication and support for assigned clinical research protocols.
5. Will the CRA conduct site visits?
Yes. The responsibilities include validation, initiation, monitoring and close-out visits, along with remote monitoring activities.
6. What compliance standards are involved?
The role requires compliance with ICH-GCP, applicable country regulations, study protocols, sponsor SOPs and relevant quality requirements.
7. Which systems are mentioned in the job description?
The position involves maintaining information and documentation in CTMS, eTMF and other applicable systems.
8. Is salary mentioned?
No. The provided MSD job posting does not specify the salary or CTC.
9. What is the application deadline?
The listed job posting end date is October 14, 2026. MSD advises candidates to apply no later than the day before the stated end date.
10. What is the MSD requisition ID?
The requisition ID shown in the listing is R419942.
Important Note
Job availability, eligibility requirements, application deadlines and recruitment conditions can change. Candidates should verify the latest information on the official MSD careers portal before applying. This article is prepared from the provided job information and should not be treated as an official recruitment notification from MSD.