TMF Associate at Fortrea for M.Sc/B.Sc Lifescience – Apply Now Before It’s Too Late!

TMF Associate at Fortrea for M.Sc/B.Sc Lifescience – Apply Now Before It’s Too Late!

Are you looking to kickstart or grow your clinical research career? Fortrea, A top clinical research organization is hiring for the position of TMF Associate I in Bangalore. If you have a background in Life Sciences or Business and understand GCP and ICH guidelines, this is your chance to play a vital role in maintaining trial documentation and ensuring audit readiness. But hurry — only 1 day left to apply!

About the Company:

Fortrea Holdings Inc. is a leading global contract research organization (CRO) that partners with pharmaceutical, biotechnology, and medical device companies to accelerate the development of life-changing therapies. Headquartered in Durham, North Carolina, Fortrea operates in over 90 countries and employs approximately 18,000 professionals worldwide.

• Job Title: TMF Associate I
• Location: Bangalore
• Time Type: Full time
• Posted On: Today
• End Date to Apply: May 16, 2025 (1 day left to apply)
• Job Requisition ID: 252238

Job Overview:

Manages the document classification under Smart Inbox and ARC review (as applicable) as well as document deletion.

Summary of Responsibilities:

• Maintains an understanding of applicable regulatory requirements.
• Managing electronic Trial Master Files (eTMF) for clinical studies.
• Responsible for document classification, ARC review, and document deletion.
• Ensures TMF is audit-ready for quality and compliance.
• Identifies operational issues and resolutions related to the TMF.
• Prepares the TMF for audits and implements corrective actions.
• Collaborates with team members and ensures client satisfaction.
• Participates in business improvement initiatives.

Qualifications (Minimum Required):

• Bachelor’s Degree with a Life Sciences/Business focus.
• Minimum 6-12 months of experience in a clinical research environment.
• Clear understanding of GCP and ICH guidelines.
• Knowledge of Regulatory/Clinical document requirements.

Preferred Qualifications:

• Master’s Degree with a Life Sciences/Business focus.
• Equivalent experience within clinical research environment.
• Experience working in clinical electronic systems.

Physical Demands/Work Environment:

Minimal travel (less than 10%) required for meetings.

APPLY ONLINE HERE!

Keywords: TMF Associate, Clinical Research, Regulatory Requirements, GCP Guidelines, Clinical Studies, jobs, TMF Associate at Fortrea