Global healthcare company Sanofi has announced openings for the position of Clinical Trial Support Associate (CTSA) in Hyderabad, India. Candidates with qualifications in Life Sciences, Healthcare Administration, Pharmacy, Biotechnology, and related fields can apply for this exciting clinical research opportunity.
This Sanofi Clinical Trial Support Associate job is ideal for freshers and experienced professionals looking to build a career in clinical operations, clinical trial management, CTMS administration, TMF management, and clinical research support.
Job Overview
| Details | Information |
|---|---|
| Position | Clinical Trial Support Associate |
| Company | Sanofi |
| Location | Hyderabad |
| Department | R&D Clinical Operations |
| Employment Type | Full Time |
| Job ID | R2858065 |
| Application Deadline | June 30, 2026 |
About the Role
The Clinical Trial Support Associate (CTSA) plays a critical role in supporting clinical studies throughout their lifecycle. The role involves coordination with Clinical Operations Study Leaders (COSL), Global Study Leaders (GSL), and Clinical Operations Study Country Leaders (COSCL).
The selected candidate will help manage:
- Clinical trial documentation
- Trial Master File (TMF)
- CTMS administration
- Study communications
- Vendor and investigator payments
- Audit readiness activities
- Site coordination and compliance
This opportunity offers strong exposure to global clinical trial operations and international regulatory practices.
Key Responsibilities
Study Communication & Documentation
- Distribute protocol amendments and Investigator Brochure updates
- Prepare study newsletters, memos, and site communications
- Maintain ICF tracking logs and patient data reports
- Coordinate equipment leasing and insurance requests
- Track site training records and maintain study contact lists
- Archive study documentation in TMF and SharePoint systems
Financial Management
- Process investigator and vendor payment requests
- Create and manage purchase orders (POs)
- Track study budgets and invoice approvals
- Coordinate payment status reporting with study teams
CTMS & Systems Administration
- Set up and maintain CTMS at study and site levels
- Manage user access and system permissions
- Generate compliance and data quality reports
- Support digital clinical trial tools and platforms
Audit & Inspection Support
- Perform In-Process Control (IPC) checks
- Support audit and inspection readiness
- Assist with regulatory inspection documentation
- Contribute to BIMO and PAI readiness activities
Eligibility Criteria
Candidates applying for the Sanofi Clinical Trial Support Associate role should have:
- Bachelor’s degree in Life Sciences, Pharmacy, Biotechnology, Healthcare Administration, or related field
- Knowledge of clinical development and clinical operations
- Understanding of GCP, ICH Guidelines, FDA, and EMA regulations
- Good communication and documentation skills
- Strong organizational and multitasking abilities
- Familiarity with CTMS systems preferred
- Ability to adapt to digital tools and evolving processes
Preferred Qualifications
Candidates with exposure to the following areas will have an added advantage:
- Clinical trial management systems (CTMS)
- TMF management
- Vendor management
- Clinical research coordination
- Financial tracking in clinical studies
- Audit and inspection readiness support
Salary Expectations
Based on industry standards for Clinical Trial Support Associate jobs in Hyderabad, the estimated salary range is:
- ₹4.5 LPA – ₹8 LPA (depending on experience and skills)
Why Join Sanofi?
Working at Sanofi provides employees with opportunities to contribute to innovative healthcare research and global clinical development programs.
Benefits Include
- Global clinical research exposure
- Career growth in clinical operations
- Collaborative international work environment
- Learning opportunities in regulatory compliance
- Experience with advanced clinical trial technologies
How to Apply
