CRA Job Opportunity At Syngene Career | Apply Now
Looking for a CRA Job in Bangalore? Syngene career is hiring for the position of CRA II (Clinical Research Associate) in its Clinical Operations team. This role is ideal for M.Pharm, M.Sc, Pharm D, and life science professionals with experience in clinical monitoring and site management. The position focuses on clinical trial monitoring, GCP compliance, and end-to-end site coordination across clinical studies.
- Job Title: CRA II (Clinical Research Associate)
- Location: Bangalore, India
- Department: Clinical Operations – T&CR
About the Company
Syngene is an innovation-led contract research organization offering integrated scientific services across discovery, development, and manufacturing. The company works with global pharmaceutical and biotechnology clients to deliver high-quality research solutions. Syngene is known for its strong focus on safety, quality compliance, and scientific excellence, making it a leading name in clinical research and contract research services in India.
Job Description
In this CRA II Job at Syngene Career, the candidate will be responsible for site selection, initiation, monitoring, and close-out activities for clinical trials. The role involves ensuring compliance with Good Clinical Practice (GCP), managing site performance, and maintaining high-quality data integrity. The CRA will coordinate with investigators and clinical teams, ensure timely regulatory approvals, monitor patient recruitment, review CRF data, and support resolution of clinical data queries while maintaining study documentation and compliance standards.
Key Responsibilities
- Conduct site selection, initiation, monitoring, and close-out visits
- Ensure compliance with GCP guidelines and SOPs
- Manage investigator sites and maintain regular communication
- Track regulatory and ethics committee approvals
- Monitor subject recruitment and study progress
- Review and ensure accurate CRF completion
- Manage data queries and resolution processes
- Submit monitoring visit reports and follow-up letters
- Ensure quality and integrity of clinical trial data
- Maintain complete study documentation
- Coordinate with Clinical Project Managers for issue resolution
Eligibility Criteria For CRA Job
- Education: M.Pharm / M.Sc / Pharm D
- Experience: Experience as Senior CRA or CRA II preferred, Strong background in clinical operations and site monitoring, Hands-on exposure to clinical trial execution and GCP compliance
Required Skills
- Clinical Trial Monitoring
- Good Clinical Practice (GCP)
- Site Management & Coordination
- Clinical Documentation & Reporting
- Regulatory Compliance
- CRF Review & Data Management
- Communication & Stakeholder Management
- Time Management & Multitasking
- Problem Solving in Clinical Operations
- Team Collaboration
This CRA II Job at Syngene Career is a great opportunity for clinical research professionals to advance their careers in clinical operations and trial monitoring. The role provides hands-on exposure to GCP-compliant studies, site management, and global clinical research processes. If you are looking to grow in clinical research and contribute to high-quality clinical trials, this position in Bangalore offers strong career growth in a leading research organization.
