TMF Associate at Fortrea for M.Sc/B.Sc Lifescience - Apply!
--Must See--

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

Shekhar
Shekhar Suman is the Co-founder of BioTecNika Info Labs Pvt. Ltd. He is an Entrepreneur, Writer, Public Speaker, and a Motivational Coach. In his career, he has mentored more than 100,000+ students toward success in the Biopharma Industry. He heads the BioTecNika Group, which comprises BioTecNika.com, BioTecNika.org, and Rasayanika.com. An avid reader and listener who is passionate about BioSciences. Today Biotecnika is India's largest Biotech Career portal, with over 5 Million subscribers from academia & Industry. It's ranked among the top 50 websites worldwide in the Biology category.

LEAVE A REPLY

Please enter your comment!
Please enter your name here