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Syngene International Ltd. is hiring a Clinical Research Associate (CRA) for its Clinical Operations team in Bangalore. This opportunity is ideal for professionals with hands-on experience in core clinical research activities, site monitoring, and ICH-GCP compliance who are looking to grow their career with a globally recognized contract research and discovery services organization.
With a strong presence in drug discovery, development, and manufacturing, Syngene collaborates with global leaders such as Bristol-Myers Squibb, Baxter, Amgen, GSK, and Merck KGaA. Joining Syngene means contributing to high-quality clinical research while working in a scientifically driven and compliance-focused environment.
Job Details
- Job Title: Clinical Research Associate
- Department: Clinical Operations
- Division: Discovery Services
- Location: Bangalore, India
- Job Type: Full-time
- Industry: Clinical Research / CRO
- Date Posted: 18 December 2025
Key Responsibilities – Clinical Research Associate
- Conduct site selection, initiation, monitoring, and close-out visits as per protocol, SOPs, and ICH-GCP guidelines
- Act as the primary liaison between clinical trial sites and project teams
- Ensure protocol compliance, data quality, and subject safety at site level
- Track Ethics Committee and regulatory submissions, approvals, and renewals
- Monitor subject recruitment, CRF completion, and query resolution
- Prepare and submit monitoring visit reports, follow-up letters, and site documentation
- Support CAPA implementation in coordination with the Clinical Project Manager
- Assist in development of study tools, documents, and processes
- Participate in internal and external audits
- Provide project coordination support and delegated CPM-level responsibilities when required
Educational Qualification
- Master’s Degree in Life Sciences
- Master’s in Pharmacology
Required Experience & Skills
Technical / Functional Skills
- Strong knowledge of ICH-GCP and Indian regulatory guidelines
- Experience in core clinical research and site monitoring activities
- Proficiency in MS Word, Excel, and PowerPoint
- Exposure to SOP development and compliance management
- Experience handling internal and external regulatory audits
Behavioral Skills
- Excellent English communication (reading & writing)
- Strong stress management and conflict resolution skills
- Empathy, patience, and professional site relationship management
Why Join Syngene? (Benefits & Growth)
- Work with a global innovation-focused CRO
- Exposure to international clinical trials
- Strong training culture in GCP, protocols, and therapeutic areas
- Career growth in clinical operations and project management
- Equal opportunity employer with inclusive workplace policies
How to Apply
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