Life Science Job at Syneos Health Hyderabad
Looking to build a career in clinical research and documentation? This Life Science Job at Syneos Health offers an exciting opportunity to work as a TMF Specialist in a globally recognized organization. If you are searching for an opportunity for life science graduates to enter the clinical trials domain, this role provides hands-on exposure to Trial Master File operations and regulatory processes.
About Syneos Health
Syneos Health is a leading global life sciences organization that provides integrated clinical and commercial solutions. With a strong presence worldwide, Syneos Health helps accelerate drug development and improve patient outcomes. It offers excellent Life Science Job opportunities, including roles like TMF Specialist, making it a top choice for professionals seeking an opportunity for life science graduates.
Job Details
- Job Title: TMF Specialist I (Trial Master File Operations)
- Job ID: 25107822
- Location: Hyderabad, India (Hybrid)
- Company: Syneos Health
- Job Type: Full-Time
- Work Mode: Hybrid
Role Overview
The TMF Specialist I is responsible for supporting the setup, maintenance, and close-out of the Trial Master File (TMF) in compliance with regulatory standards and client requirements. The role ensures that clinical trial documentation is accurate, complete, and inspection-ready throughout the study lifecycle.
Key Responsibilities
- Process study documentation in accordance with SOPs, Work Instructions, ICH-GCP, and regulatory guidelines
- Support TMF setup, maintenance, and closure activities across assigned studies
- Perform document scanning, indexing, filing, and uploading in electronic TMF (eTMF) systems
- Ensure security, accuracy, and compliance of TMF documentation for active and archived studies
- Conduct quality reviews of TMF documents submitted by study teams
- Perform completeness checks against expected document lists to identify gaps
- Maintain inspection readiness of TMF documentation throughout the clinical trial lifecycle
Candidate Profile
The ideal candidate is detail-oriented, organized, and familiar with clinical trial documentation processes. The individual should be capable of managing multiple tasks efficiently in a dynamic clinical research environment.
Educational Qualification
Bachelor’s or Master’s degree in Life Sciences or related field (B.Sc., M.Sc.)
Experience
- Minimum 1+ year of experience as an eTMF Specialist
- OR
- Minimum 2+ years of experience as a Clinical Research Coordinator (CRC) or in a clinical research environment
Key Skills & Competencies
- Understanding of clinical trial documentation and regulatory guidelines (ICH-GCP)
- Familiarity with medical terminology and TMF processes
- Experience with electronic TMF systems (preferred)
- Strong communication skills (verbal and written)
- High attention to detail and quality-focused mindset
- Ability to manage multiple priorities and meet deadlines
- Proficiency in Microsoft Office and Adobe Acrobat
- Ability to work independently and collaboratively in a team
Work Environment
- Hybrid clinical operations role based in Hyderabad
- Collaborative and global team environment
- Exposure to end-to-end clinical trial documentation processes
Why Join
- Opportunities for career growth and professional development
- Inclusive and collaborative workplace culture
- Exposure to global clinical research projects
- Strong focus on innovation and patient impact
Application Deadline: May 25, 2026.
