Looking to advance your career as a Clinical Research Associate (CRA) in India? A leading global biopharma company, Bristol Myers Squibb (BMS), is hiring experienced professionals in Mumbai. This opportunity is ideal for candidates with 2โ3 years of clinical research experience, strong knowledge of ICH-GCP guidelines, and hands-on exposure to clinical trial systems like CTMS, eTMF, and EDC.
This Clinical Research Associate job in Mumbai offers the chance to work on cutting-edge clinical trials while ensuring compliance, patient safety, and data integrity.
Job Overview
- Role: Clinical Research Associate (CRA)
- Location: Mumbai, Maharashtra, India
- Experience: 2โ3 Years
- Company: Bristol Myers Squibb
- Job Type: Full-Time
- Requisition ID: R1601665
- Posted On: April 23, 2026
Key Responsibilities
As a Clinical Research Associate, you will:
- Conduct site qualification, initiation, monitoring, and close-out visits
- Ensure compliance with ICH-GCP guidelines, SOPs, and regulatory requirements
- Perform source data verification (SDV) to ensure data accuracy and integrity
- Monitor clinical trial sites for protocol adherence and patient safety
- Support audit and inspection readiness for regulatory authorities
- Build strong relationships with investigators, vendors, and stakeholders
- Analyze site performance metrics and implement risk-based monitoring strategies
- Manage study drug accountability (IMP) and documentation
- Assist in Ethics Committee submissions and ICF reviews
- Prepare monitoring reports and documentation in a timely manner
Required Qualifications
- Bachelorโs degree in Life Sciences / Pharmacy / related field
- Valid driverโs license (if required for travel)
Required Experience
- 2โ3 years of Clinical Research Associate experience
- Experience in pharma/biotech sponsor or CRO environment
- Understanding of clinical trial lifecycle and drug development process
Key Skills & Competencies
- Strong knowledge of ICH-GCP, regulatory guidelines, and ALCOA principles
- Hands-on experience with:
- CTMS (Clinical Trial Management Systems)
- eTMF (Electronic Trial Master File)
- EDC (Electronic Data Capture systems)
- RBQM tools like Veeva, Medidata, CluePoints
- Excellent analytical and risk assessment skills
- Strong communication and stakeholder management
- Ability to work independently across multiple protocols
Salary & Benefits
- Estimated Salary: โน8 โ โน14 LPA (based on experience and industry standards)
- Competitive benefits including:
- Health & wellness programs
- Flexible work model (site-based / hybrid depending on role)
- Career growth and global exposure
- Learning & development opportunities
Why Join Bristol Myers Squibb?
- Work with a globally recognized biopharma leader
- Be part of life-changing clinical research innovations
- Exposure to advanced clinical trial technologies and methodologies
- Strong focus on employee growth, inclusion, and innovation
How to Apply
