Associate – Regulatory Affairs
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Clinical Research Associate
 Location: Mumbai, Maharashtra, India
Job ID: Not specifiedCompany: Bristol Myers Squibb (BMS)
Employment Type: Full-time (On-site / Field-based)
Job Overview
At Bristol Myers Squibb (BMS), every role contributes to our mission of transforming patients’ lives through science™. As a Clinical Research Associate (CRA), you will act as the primary site-level contact for internal and external stakeholders, ensuring clinical trial sites operate with the highest standards of quality, integrity, and compliance. This position offers a chance to grow your career through meaningful, life-changing work that advances global health.
Role & Responsibilities
- Conduct site qualification, initiation, routine monitoring, and close-out visits in accordance with protocol, SOPs, and ICH-GCP.
- Verify accuracy, completeness, and integrity of data within electronic and paper records.
- Monitor site adherence to ICH-GCP and local regulatory guidelines; provide training and guidance to ensure compliance and patient safety.
- Build and maintain effective relationships with investigators, clinical sites, vendors, and internal teams.
- Motivate and support sites to achieve enrollment and retention goals.
- Prepare timely and professional reports following monitoring visits.
- Participate in regulatory audits, inspections, and corrective/preventive action implementation.
Educational Qualification
- Bachelor’s degree (preferably in Life Sciences or equivalent).
- 2–3 years of relevant clinical research experience as a CRA.
- Prior pharma or biotech sponsor experience preferred.
- In-depth understanding of clinical research processes, ICH-GCP, and local regulatory requirements.
- Valid driver’s license (as locally required).
Location
 Mumbai, Maharashtra, India
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