Life Science Jobs at Syneos Health
Searching for the latest Life Science Jobs in clinical research? Syneos Health Jobs has announced an exciting opening for a TMF Specialist I in Hyderabad. This hybrid opportunity is ideal for candidates with experience in Clinical Research Coordination (CRC) or electronic Trial Master File (eTMF) management. If you’re looking for an opportunity for life science graduates to build a successful career in global clinical trials and regulatory documentation, this position deserves your attention.
About the Company
Syneos Health is a globally recognised, fully integrated life sciences services organisation that supports pharmaceutical, biotechnology, and medical device companies throughout the drug development and commercialisation lifecycle. With more than 25,000 professionals worldwide, Syneos Health combines clinical research expertise, commercial capabilities, and technology-driven solutions to accelerate the delivery of innovative healthcare products to patients around the world.
Job Details:
- Position: TMF Specialist I
- Organisation: Syneos Health
- Location: Hyderabad, India
- Work Mode: Office-based (Hybrid)
- Job Type: Full-time
- Application Deadline: 03 July 2026
Job Summary
The TMF Specialist I is responsible for supporting the set-up, maintenance, and close-out of the Trial Master File (TMF) in compliance with client requirements, internal procedures, and global regulatory standards.
The role contributes to maintaining inspection-ready Trial Master File documentation throughout the clinical trial lifecycle.
Experience
Minimum 1+ years of experience in:
- Electronic Trial Master File (eTMF)
- OR
- Clinical Research Coordinator (CRC)
- OR
- Clinical research environment with understanding of clinical trial documentation and applicable regulatory guidelines.
Key Responsibilities
The selected candidate will:
- Process study documentation in accordance with:
- Standard Operating Procedures (SOPs)
- Work Instructions
- ICH-GCP guidelines
- Regulatory guidelines
- Study-specific requirements
- Support Trial Master File (TMF) setup, maintenance, and closure activities across assigned studies.
- Perform document scanning, indexing, filing, and uploading in electronic Trial Master File (eTMF) systems.
- Ensure the security, accuracy, and compliance of TMF documents for both active and archived studies.
- Conduct Quality Reviews of Trial Master File documents submitted by study teams.
- Perform Completeness Reviews against Expected Document Lists to identify missing or incomplete TMF documentation.
Educational Qualification
Candidates should possess any one of the following qualifications Bachelor’s degree/ Master’s degree in Life Sciences or a related field
Required Skills
Candidates should have:
- Familiarity with medical terminology.
- Understanding of Trial Master File (TMF) processes.
- Experience with electronic Trial Master File (eTMF) systems (advantage).
- Strong verbal and written communication skills.
- Excellent attention to detail.
- Strong organizational skills.
- Quality-focused mindset.
- Ability to prioritize multiple tasks and meet deadlines in a dynamic environment.
- Proficiency in:
- Microsoft Office Suite
- Adobe Acrobat
Ability to work effectively both independently and as part of a team.
