Are you a detail-oriented and organized professional looking for a challenging role in clinical research? We are hiring an R&D eTMF Document Specialist in Hyderabad, and this could be the perfect opportunity for you to build a successful career in the pharmaceutical industry. 🌟
About the Role 📝
As an R&D eTMF Document Specialist, you will play a crucial role in managing the Trial Master File (TMF) documentation system, ensuring compliance with regulatory requirements and internal processes throughout the lifecycle of clinical studies. Your responsibilities will include:
- TMF Document Management: Manage TMF documents in accordance with internal processes and applicable regulations.
- Documentation Activities: Perform documentation activities across all levels within a study (study, country, and site).
- Quality Control: Perform independent quality control of documents submitted to the TMF.
- Collaboration: Collaborate with study teams, TMF managers, and other stakeholders to ensure proper documentation practices are followed.
Requirements 📚
- Education: Bachelor’s degree in Life Sciences, Pharmacy, or related field.
- Experience: Experience in eTMF management or clinical documentation is a plus.
- Knowledge: Knowledge of ICH-GCP, regulatory requirements, and clinical development process.
- Skills: Strong attention to detail and organizational skills, excellent written and verbal communication skills in English.
What You Can Expect 🌟
- Career Growth: Opportunities for career growth and professional development.
- Collaborative Team: Work with a team of experienced professionals who share your passion for clinical research.
- Competitive Salary: A competitive salary and benefits package.
- Learning Opportunities: Opportunities to learn and develop new skills.
Why Choose This Role? 🤔
- Industry Leader: Opportunity to work with a leading company in the pharmaceutical industry.
- Innovative Solutions: Opportunity to work on innovative solutions that transform healthcare and improve patient outcomes.
- Diverse Workforce: Work with a diverse team of professionals from different backgrounds and industries.
How to Apply 📧
If you’re interested in this exciting opportunity, please submit your application before December 31, 2025. You can apply online through the below Link 👇🏻:
https://sanofi.wd3.myworkdayjobs.com/en-US/SanofiCareers/job/Hyderabad/R-D-eTMF-Document-Specialist_R2832264?shared_id=818655b4-85bc-4866-91a9-0d5980d083f2
Tips for eTMF Document Specialists 📝
- Develop Strong Organizational Skills: Develop strong organizational skills to effectively manage TMF documents.
- Stay Current: Stay up-to-date with the latest developments and trends in clinical research and eTMF management.
- Improve Your Communication Skills: Improve your communication skills to effectively collaborate with study teams and stakeholders.
Benefits of Working in eTMF Management 🌟
- Career Growth: Opportunities for career growth and professional development.
- Competitive Salary: A competitive salary and benefits package.
- Variety: Opportunity to work on different clinical trials and therapeutic areas.
I’m actively looking for opportunity in eTMF.
Thank you for your comment! If you’re actively looking for opportunities in eTMF, we recommend keeping an eye on current openings posted in the clinical research and documentation domain. We will continue sharing relevant job updates, so stay connected with our site for the latest eTMF and TMF-related roles.
Activity looking ETMF role
Thank you for your interest!
If you are actively looking for an eTMF (Electronic Trial Master File) role, you’re in the right place. We regularly share the latest openings in Clinical Research, eTMF Management, TMF Operations, and related domains.
👉 Stay tuned to our job updates section for fresh opportunities.
👉 You can also drop your resume or connect with us for upcoming eTMF positions.
We appreciate your engagement and wish you the best in securing the right eTMF role soon!