MSD Pharmaceuticals Pvt Ltd is hiring experienced candidates for the position of Specialist, Clinical Research Associate (CRA) in Mumbai, Maharashtra. This is an excellent opportunity for professionals looking to build a career in clinical research, clinical trial monitoring, and site management with one of the world’s leading pharmaceutical companies.
The company is looking for candidates with strong expertise in ICH-GCP guidelines, clinical trial monitoring, regulatory compliance, clinical site management, and protocol adherence. Candidates with experience in handling remote and on-site monitoring activities, audit readiness, and investigator communication are encouraged to apply.
Job Highlights
| Particulars | Details |
|---|---|
| Company | MSD Pharmaceuticals Pvt Ltd |
| Job Role | Specialist, Clinical Research Associate |
| Job Location | Mumbai, Maharashtra |
| Employment Type | Full Time |
| Experience | Experienced Professionals |
| Industry | Clinical Research / Pharmaceutical |
| Application Deadline | 30 May 2026 |
| Job ID | R398007 |
Key Responsibilities
The selected candidate will be responsible for:
- Managing clinical trial sites and ensuring compliance with ICH-GCP and sponsor SOPs
- Conducting site monitoring visits including initiation, monitoring, validation, and close-out visits
- Maintaining strong relationships with investigators and site staff
- Reviewing and managing regulatory documentation for study start-up and close-out
- Ensuring subject safety, protocol adherence, and data integrity
- Supporting audit and inspection readiness activities
- Identifying and resolving site performance and compliance issues
- Managing documentation in CTMS, eTMF, and other clinical systems
- Supporting CRA mentoring, co-monitoring visits, and knowledge sharing
- Collaborating with regulatory affairs, pharmacovigilance, finance, legal, and regional teams
Required Skills
Candidates applying for this CRA job in Mumbai should possess:
- Clinical Trials Monitoring experience
- Good Clinical Practice (GCP) knowledge
- Clinical Site Management expertise
- Regulatory Compliance understanding
- Clinical Study Management skills
- Protocol Adherence knowledge
- Adverse Event Reporting System understanding
- Data Analysis and Reporting skills
- Strong communication and teamwork abilities
- Adaptability and accountability
Educational Qualification
Candidates from the following backgrounds are preferred:
- B.Pharm
- M.Pharm
- Pharm.D
- Life Sciences
- Clinical Research related disciplines
Preferred Experience
- Experience in clinical trial site monitoring
- Knowledge of ICH-GCP guidelines
- Experience handling regulatory documentation and audit support
- Ability to conduct remote and on-site monitoring visits
- Familiarity with CTMS and eTMF systems
Salary & Benefits
MSD offers competitive salary packages and career growth opportunities in global clinical research operations.
Expected Salary Range
- ₹8 LPA – ₹18 LPA (Expected)
Employee Benefits
- Global exposure in clinical trials
- Career growth opportunities
- Training and mentoring programs
- Collaborative work environment
- Exposure to regulatory and audit processes
Job Location
Mumbai, Maharashtra, India