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Syngene Hiring CTA – Clinical Operations (ClinOps) | Freshers / 0–2 Years
Syngene
Bangalore
0–2 Years
Clinical Operations
Clinical Research
CTA Role
🏢 About Syngene
Syngene International Ltd. is a global contract research, development, and manufacturing organization (CRDMO) providing integrated scientific services from discovery to commercial supply. The company supports pharmaceutical, biotechnology, and healthcare companies worldwide.
📌 Job Overview
- Role: CTA – Clinical Operations (CTA-ClinOps)
- Company: Syngene International Ltd.
- Location: Bangalore
- Department: Clinical Operations – T&CR
- Experience: 0–2 Years
- Employment Type: Full-Time
🔬 Key Responsibilities
- Maintain Trial Master File (TMF) and Investigator Site Files (ISF)
- Support Clinical Study Managers and CRAs in trial coordination
- Track regulatory approvals and study milestones
- Manage clinical documentation and study logs
- Assist with regulatory and ethics committee submissions
- Coordinate investigator meetings and monitoring visits
- Manage clinical data flow and update CTMS systems
- Assist with clinical trial supply management and shipment tracking
- Prepare documentation for audits and inspections
- Ensure compliance with ICH-GCP guidelines and SOPs
🎓 Eligibility Criteria
- M.Sc (Life Sciences)
- M.Pharm
- Pharm.D
- BAMS / BHMS / BDS / MDS
- Any Life Science degree
- Understanding of clinical research and GCP guidelines
- Strong documentation and coordination skills
⭐ Why Join Syngene?
- Exposure to global clinical research projects
- Opportunity to work with experienced clinical teams
- Career growth in Clinical Operations
- Experience in TMF management and clinical trial coordination
- Work in a regulated and innovation-driven research environment
📌 Note Before You Apply:
Kindly read the entire job description carefully before applying. Understanding clinical research documentation and GCP guidelines will improve your chances of selection.
Kindly read the entire job description carefully before applying. Understanding clinical research documentation and GCP guidelines will improve your chances of selection.
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