Syngene is hiring Senior Clinical Research Associate (Sr. CRA) in Bangalore. This is a great opportunity for experienced clinical research professionals seeking pharma jobs, clinical research jobs, and CRO careers in India.
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About the Company
Syngene International is an innovation-led Contract Research, Development and Manufacturing Organization (CRDMO) offering integrated scientific services from early discovery to commercial supply.
As a leading player in the life sciences sector, Syngene supports global pharmaceutical and biotech companies with high-quality research and development services. The company places strong emphasis on safety, quality, integrity, and operational excellence, providing a dynamic environment for professionals to grow in clinical operations.
Job Details
- Company Name: Syngene International
- Experience: Experience as Senior Clinical Research Associate (Sr. CRA) required
- Qualification: M.Sc / M.Pharm / Pharm.D / BAMS / BDS / MDS / BHMS or any Life Sciences degree
- Location: Bangalore, Karnataka
- Work Type: Full time (On-site)
Job Description
Syngene is looking for a Senior Clinical Research Associate to join the Clinical Operations – T&CR team in Bangalore. The role involves end-to-end site management, monitoring, and ensuring compliance with GCP guidelines for clinical trials.
Senior Clinical Research Associate
- Department: Clinical Operations – T&CR
- Division: Discovery Services
- Role: Senior Clinical Research Associate
- Experience: Sr. CRA level experience required
- Education/Qualification: M.Sc, M.Pharm, Pharm.D, BAMS, BDS or equivalent life sciences degree
Skills/Qualifications
- Good communication skills and ability to work as a strong team player
- Experience in site selection, initiation, monitoring, and close-out visits
- Thorough knowledge of GCP guidelines and regulatory requirements
- Ability to work in a dynamic and ambiguous environment
- Strong problem-solving and prioritization skills
- Ability to meet tight deadlines and develop creative solutions
- Proficiency in clinical trial documentation and reporting
Key Responsibilities
- Perform site selection, initiation, monitoring, and close-out visits per SOPs and GCP
- Manage assigned study sites and therapeutic areas
- Ensure quality and integrity of study data at site level
- Track regulatory submissions, Ethics Committee approvals, subject recruitment, and CRF completion
- Investigate quality issues and implement CAPA
- Prepare monitoring visit reports, follow-up letters, and other study documentation
- Administer protocol training to site teams
- Maintain regular communication with sites and project managers
- Submit timesheets and complete all mandatory training on time
Benefits/Perks
- Work with a leading global CRDMO
- Exposure to diverse clinical trials and therapeutic areas
- Strong focus on professional development and safety culture
- Collaborative and innovative work environment
- Opportunities for career growth in clinical research
- Equal opportunity employer with inclusive policies
How to Apply
Interested candidates can apply for the Senior Clinical Research Associate position at Syngene Bangalore through the official Syngene career portal or by visiting www.syngeneintl.com.
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Verification: To confirm the legitimacy of this posting, you can view the original announcement on the Syngene Career page.

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Apply promptly to join Syngene’s Clinical Operations team.
Why You Should Join
Syngene offers a purpose-driven career where your work contributes to innovative drug development and improved patient outcomes. Benefit from a strong safety-first culture, global exposure, and opportunities to work on cutting-edge research projects.
The company values excellence, integrity, and professionalism, making it an ideal place for long-term growth in the clinical research domain.
FAQs
What is the location of the Syngene Sr. CRA job?
Bangalore, Karnataka.
What qualifications are required for this role?
M.Sc, M.Pharm, Pharm.D, BAMS, BDS or any life sciences degree with relevant clinical research experience.
Is prior experience as Sr. CRA mandatory?
Yes, candidates with experience as Senior Clinical Research Associate are preferred.
What are the key focus areas of this position?
Site monitoring, clinical trial management, GCP compliance, and site relationship management.
Does Syngene provide equal employment opportunity?
Yes, Syngene is an Equal Opportunity Employer and provides reasonable accommodations for qualified individuals.