Looking for the latest Syngene CRA Jobs 2026? Syngene International is hiring a Specialist โ Clinical Trials (Clinical Research Associate – CRA) for its Clinical Operations team in Bangalore. This opportunity is ideal for experienced clinical research professionals with hands-on expertise in site monitoring, GCP compliance, clinical trial management, and site coordination.
If you have a Master’s Degree in Life Sciences or Pharmacology and practical experience in clinical research activities, this Syngene Clinical Research Associate job offers an excellent opportunity to advance your career with one of India’s leading contract research organizations (CROs).
About Syngene
Syngene International is an innovation-driven Contract Research, Development, and Manufacturing Organization (CRDMO) providing integrated scientific services from drug discovery to commercial manufacturing. The company partners with leading pharmaceutical, biotechnology, and healthcare organizations worldwide while maintaining the highest standards of quality, safety, and regulatory compliance.
Job Details
| Particular | Details |
|---|---|
| Position | Specialist โ Clinical Trials |
| Role | Clinical Research Associate (CRA) |
| Company | Syngene International |
| Department | Clinical Operations |
| Job Location | Bangalore, Karnataka |
| Employment Type | Full-Time |
| Experience | Experienced CRA |
| Qualification | Master’s Degree in Life Sciences or Master’s in Pharmacology |
Key Responsibilities
As a Clinical Research Associate (CRA) at Syngene, you will:
- Perform site selection, initiation, monitoring, and close-out visits.
- Ensure compliance with Good Clinical Practice (GCP), SOPs, and regulatory guidelines.
- Manage assigned clinical trial sites and study protocols.
- Conduct protocol and study-related training for investigators and site staff.
- Monitor study progress, patient recruitment, and regulatory submissions.
- Review Case Report Forms (CRFs) and resolve data queries.
- Prepare monitoring reports, follow-up letters, and site documentation.
- Identify quality issues and support CAPA implementation.
- Coordinate with Clinical Project Managers on study execution.
- Support development of study tools, documentation, and operational processes.
- Submit project documentation and timesheets on schedule.
- Ensure adherence to Syngene’s Environment, Health & Safety (EHS) standards.
Educational Qualification
Candidates should possess:
- Master’s Degree in Life Sciences
OR - Master’s Degree in Pharmacology
Experience Required
Applicants should have:
- Hands-on Clinical Research Associate (CRA) experience
- Practical experience in core clinical research operations
- Strong knowledge of:
- ICH-GCP Guidelines
- Clinical Trial Monitoring
- Regulatory Compliance
- Site Management
- Clinical Documentation
- Ethics Committee processes
Preferred Skills
- Clinical Trial Monitoring
- Site Initiation Visits (SIV)
- Site Close-Out Visits (COV)
- Regulatory Documentation
- Case Report Forms (CRF)
- Clinical Data Review
- Communication & Coordination
- Time Management
- Quality Assurance
- CAPA Management
- Clinical Operations
Why Join Syngene?
Working at Syngene offers several career advantages:
- Opportunity to work on global clinical trials
- Exposure to multinational pharmaceutical projects
- Strong learning and career development programs
- Collaborative scientific work environment
- Industry-leading safety culture
- Professional growth within Clinical Operations
- Equal employment opportunity workplace
- Continuous training in GCP, EHS, and regulatory compliance
Expected Salary
Based on current market standards for experienced Clinical Research Associates in Bangalore:
Estimated Salary: โน7,00,000 โ โน12,00,000 per annum (CTC)
Actual compensation will depend on candidate experience, qualifications, and internal company policies.
How to Apply
