Fortrea Jobs | Apply Today for Senior TMF Associate Role to unlock your Clinical Research Careers!
Join for a Senior TMF Associate Role, working remotely from Mumbai, managing electronic Trial Master Files (eTMF) and ensuring audit readiness. Ideal for professionals with 3–6 years’ clinical research experience looking to advance in clinical research careers by document management and compliance.
About Fortrea:
Fortrea is a leading clinical research organization dedicated to helping clients accelerate the development of life-changing therapies. With a strong focus on quality and compliance, Fortrea is committed to providing exceptional service to support the advancement of cutting-edge medical treatments.
Job Description:
- Job Posting: Senior TMF Associate
- Location: Mumbai, India (Remote)
- Job Type: Full-time
- Posted On: Yesterday
- End Date to Apply: November 30, 2025
- Job Requisition ID: 255324
- Work Environment: Minimal travel (<10%) for meetings as required
Educational Requirements for this Senior TMF Associate Role:
- Bachelor’s Degree in Life Sciences or Business (required)
- Master’s Degree in Life Sciences or Business preferred or equivalent clinical research experience (3–6 years)
Key Responsibilities for this Senior TMF Associate Role:
- In this Senior TMF Associate Role, you have to manage eTMF documents, including classification, review, and deletion under Smart Inbox and ARC processes.
- Ensure TMF audit readiness through visual quality and audit-ready checks.
- Track and process essential study artifacts per SOPs, sponsor requirements, GCP, and ICH guidelines.
- Identify and resolve operational issues within TMF management.
- Prepare TMF for QA or sponsor audits, implementing corrective actions as required.
- Participate in internal and client audits.
- Collaborate with BP&S teams and maintain client satisfaction.
- Engage in business improvement initiatives, training, and mentoring.
- Attend internal or external study team meetings as needed.
Skills Required for this Senior TMF Associate Role:
- 3–6 years of clinical research experience
- Strong knowledge of GCP and ICH guidelines
- Understanding of regulatory and clinical document requirements
- Proficiency in Microsoft Office, web-based applications, and Adobe Acrobat
- Excellent interpersonal and communication skills
- Experience with clinical electronic systems preferred
How to Apply for Fortrea Jobs?
Interested candidates can apply online before November 30, 2025. Keep an eye on official company alerts for updates on the recruitment process.
Career Opportunities After Senior TMF Associate Role:
- TMF Lead / Specialist – Oversee TMF compliance and audits.
- Clinical Documentation Manager – Manage study documents and regulatory compliance.
- Clinical Research Associate (CRA) – Monitor sites and ensure study compliance.
- Quality Assurance / Regulatory Roles – QA Specialist, Regulatory Affairs Associate.
- Clinical Project Coordinator / Manager – Supervise trial operations and timelines.
- eTMF / Clinical Systems Specialist – Manage electronic trial systems and workflows.
- Operations / Process Improvement Lead – Improve TMF workflows and efficiency.
