Life Science Jobs in Hyderabad: Sanofi is Hiring | Apply Now
If you’re looking to grow your career in clinical research and documentation, Sanofi is offering an exciting opportunity for life science graduates to join as an R&D eTMF Document Specialist in Hyderabad. This role is perfect for candidates aspiring to build a strong future in life science jobs, with the added advantage of becoming part of a globally trusted organization. A Sanofi career is known for innovation, impact, and exceptional learning and this opening is one of the most promising life science jobs in Hyderabad.
Job Details
- Job Title: R&D eTMF Document Specialist
- Location: Hyderabad
About the Company
Sanofi is a global biopharmaceutical and healthcare company renowned for its commitment to scientific innovation, patient well-being, and global health impact. With operations spanning over 100 countries, Sanofi develops and delivers life-changing therapies across a wide range of therapeutic areas — from vaccines and specialties to rare diseases and general medicine.
For professionals seeking rewarding life science jobs, Sanofi offers a dynamic environment where cutting-edge research meets compassionate care. Their teams are built on collaboration, diversity, and a shared mission to improve lives worldwide. This makes Sanofi a top employer for
individuals looking for a meaningful and progressive Sanofi career.With growing operations in India — including Hyderabad — and increasing focus on clinical research and documentation excellence, Sanofi presents excellent opportunities for life science jobs in Hyderabad. Whether you are a fresh graduate or an experienced professional, joining Sanofi means contributing to global healthcare advancements while building long-term growth in a trusted and respected organization.
Key Responsibilities
1. TMF Document Management
- Manage and file TMF documents in compliance with regulatory and internal standards
- Perform metadata checks, QC reviews, and indexing verification
- Conduct Expected Document List (EDL) checks and follow-up on missing items
- Coordinate user task management and ensure TMF completeness across all levels
- Identify inconsistencies, manage corrections, and escalate recurring issues
- Collaborate with TMF managers, COSLs, COSCLs, Study Leaders, and Site Monitors
2. Quality & Compliance Support
- Conduct independent document QC
- Support audits and regulatory inspection preparations
- Assist with document retrieval during inspections
3. Process Improvement
- Support continuous improvement initiatives
- Contribute to new system enhancements, testing, and training material development
- Track TMF metrics and quality indicators
4. Cross-Functional Collaboration
- Coordinate with vendors, CROs, and global study teams
- Maintain communication across TMF management and operations teams
Education
- Bachelor’s degree in Life Sciences, or relevant discipline
- Experience in eTMF systems (Veeva Vault preferred) is a plus
- Strong understanding of ICH-GCP, clinical documentation, and regulatory guidelines
Skills Required
- Strong attention to detail
- Excellent communication skills
- Knowledge of eTMF systems (Veeva Vault preferred)
- Understanding of clinical development processes
- Ability to multitask in fast-paced environments
- Analytical and problem-solving skills
- Strong organizational and documentation abilities
- Adaptability to new technologies
This role is an excellent opportunity for candidates looking to grow in clinical research, documentation, and regulatory compliance. Whether you’re beginning your journey in life science jobs or aiming to advance your Sanofi career, this position offers exposure, skill development, and a chance to contribute to global scientific progress. With Sanofi’s innovative environment and the growing demand for life science jobs in Hyderabad, this opening is truly a chance to advance your future in the pharma industry.
