Looking for Clinical Research Associate Jobs in Mumbai? Merck (MSD) has announced a Clinical Research Associate (CRA) vacancy for experienced professionals in Mumbai, Maharashtra. Candidates with at least 2 years of clinical site monitoring experience in a pharmaceutical company or CRO can apply for this exciting opportunity.
This is an excellent opportunity for professionals seeking Clinical Research Associate Jobs 2026, CRA Jobs in India, Clinical Monitoring Jobs, and ICH-GCP Clinical Research Careers with one of the world’s leading pharmaceutical companies.
Job Overview
| Particular | Details |
|---|---|
| Company | Merck (MSD) |
| Position | Clinical Research Associate (CRA) |
| Job Type | Full-Time |
| Location | Mumbai, Maharashtra, India |
| Workplace | Office (WeWork Mumbai) |
| Experience | Minimum 2 Years |
| Qualification | Bachelor’s Degree in Science/Biology or related field |
| Application Deadline | 8 July 2026 |
| Industry | Clinical Research, Pharmaceutical |
About the Role
The Clinical Research Associate is responsible for ensuring the successful execution of clinical trials while maintaining compliance with ICH-GCP, regulatory guidelines, company SOPs, and study protocols.
The selected candidate will manage assigned clinical trial sites, conduct monitoring visits, ensure patient safety, verify data quality, and collaborate with investigators and internal stakeholders throughout all phases of clinical studies.
Key Responsibilities
- Perform clinical site monitoring in accordance with ICH-GCP guidelines.
- Manage assigned clinical trial sites from initiation to close-out.
- Build strong relationships with investigators and site staff.
- Conduct Site Selection, Site Initiation, Monitoring, and Close-out Visits.
- Verify accuracy, completeness, and integrity of clinical trial data.
- Ensure subject safety, protocol compliance, and regulatory adherence.
- Maintain documentation in CTMS, eTMF, and other clinical systems.
- Resolve site performance and compliance issues.
- Support regulatory inspections and audits.
- Identify and develop new clinical research sites.
- Collaborate with pharmacovigilance, regulatory affairs, finance, legal, and global clinical teams.
- Mentor junior team members and contribute as a process SME when required.
Required Qualifications
Applicants should possess:
- Bachelor’s degree in Science, Biology, Pharmacy, Life Sciences, or a related discipline.
- Minimum 2 years of direct Clinical Research Associate (CRA) or site monitoring experience.
- Strong understanding of:
- ICH-GCP Guidelines
- Clinical Trial Monitoring
- Regulatory Compliance
- Clinical Site Management
- Good Documentation Practices
- Excellent communication and stakeholder management skills.
- Ability to work independently across multiple studies and therapeutic areas.
Preferred Skills
Successful candidates should have experience in:
- Clinical Trial Monitoring
- Clinical Site Management
- CTMS
- eTMF
- Pharmacovigilance
- Regulatory Affairs
- Root Cause Analysis
- Preventive and Corrective Actions (CAPA)
- Microsoft Office
- Clinical Data Management
- Protocol Compliance
- Patient Recruitment
- Risk Management
- Data Analysis
Why Join Merck?
Working at Merck offers numerous professional advantages:
- Global pharmaceutical organization
- Exposure to international clinical trials
- Career growth in Clinical Operations
- Opportunity to work across multiple therapeutic areas
- Collaborative global work environment
- Professional development and learning opportunities
- High-quality compliance-driven culture
Who Should Apply?
This opportunity is ideal for professionals searching for:
- Clinical Research Associate Jobs
- CRA Jobs in Mumbai
- Clinical Monitoring Jobs
- Clinical Research Careers in India
- Pharmaceutical Clinical Operations Jobs
- Clinical Trial Monitoring Jobs
- CRO Jobs India
- Experienced CRA Vacancies
- ICH-GCP Jobs
- Site Management Jobs
How to Apply
