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Senior Clinical Research Associate (Sr. Cra)

Syngene
Syngene
3-5 years
Not Disclosed
Bangalore, India
1 May 8, 2026
Job Description
Job Type: Full Time Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences Skills: Medical Billing, Medical Coding, Medical Terminology, mRS and EQ-5D-5L., Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs

Senior Clinical Research Associate (Sr. CRA) Job in Bangalore – Syngene

Company: Syngene International Ltd.
Job Title: Senior Clinical Research Associate (Sr. CRA)
Location: Bangalore, India
Department: Clinical Operations – T&CR
Job Type: Full-Time
Industry: Clinical Research / CRO / Pharmaceutical Research


About Syngene

Syngene International is a leading innovation-driven Contract Research, Development, and Manufacturing Organization (CRDMO) providing integrated scientific services from early discovery to commercial manufacturing. The company partners with global pharmaceutical, biotechnology, and healthcare organizations to accelerate research and clinical development programs.

Syngene is strongly focused on safety, operational excellence, quality compliance, and scientific innovation across all business functions.


Job Overview

Syngene is hiring a Senior Clinical Research Associate (Sr. CRA) for its Clinical Operations team in Bangalore. The selected candidate will be responsible for managing clinical trial sites, conducting monitoring visits, ensuring protocol compliance, and maintaining study quality in accordance with ICH-GCP guidelines and applicable regulatory standards.

The role requires hands-on experience in clinical trial monitoring, site management, study coordination, and clinical operations within pharmaceutical, CRO, or biotechnology environments.

This opportunity is ideal for experienced CRA professionals seeking career growth in clinical research and global clinical trial management.


Experience Required

Experience Level

  • Mid-Level to Senior-Level Clinical Research Professional
  • Freshers are not eligible

Required Experience

  • Prior experience working as a:
    • Clinical Research Associate (CRA)
    • Senior Clinical Research Associate (Sr. CRA)

Preferred Experience

  • Site monitoring
  • Clinical trial management
  • Site initiation and close-out visits
  • ICH-GCP compliance
  • Regulatory documentation
  • Clinical operations management

Educational Qualification

Required Qualification

Candidates with any of the following qualifications can apply:

  • M.Sc.
  • M.Pharm
  • Pharm D
  • BAMS
  • BDS
  • MDS
  • BHMS
  • Any Life Science Degree