Fortrea Hiring TMF Associate II – Clinical Documentation

Fortrea Hiring TMF Associate II in Bangalore – Life Sciences Graduates with 1-2 Years Experience

Fortrea invites applications for the position of TMF Associate II at its Bangalore office. Candidates with a background in Life Sciences or Business and 1–2 years of clinical research experience are encouraged to apply. The role focuses on managing eTMF documents and ensuring audit readiness, offering a promising opportunity for professionals looking to grow in the clinical documentation domain.

Fortrea TMF Associate II Job for Life Sciences Graduates with 1-2 Years Clinical Research Experience

Join Fortrea as TMF Associate II – Clinical Documentation Role in Bangalore

Are you detail-oriented and passionate about documentation in clinical trials? Fortrea is hiring TMF Associate II professionals for their clinical document management team in Bangalore. The selected candidate will be responsible for Trial Master File (TMF) management, regulatory compliance, and maintaining audit readiness in alignment with global GCP/ICH standards.

Role Overview

As TMF Associate II, you will:

• Classify documents using Smart Inbox and ARC review systems
• Perform document deletions and maintain eTMF audit readiness
• Conduct quality checks for image clarity, completeness, and regulatory compliance
• Participate in internal and client audits, audit readiness checks, and quality improvement initiatives
• Collaborate with Study Team Members and support eTMF documentation at trial, country, and site levels

Required Qualifications

Educational Background

• Bachelor’s Degree in Life Sciences or Business (Minimum)
• Master’s Degree in Life Sciences/Business (Preferred)

Experience Required

• 1–2 years’ experience in a clinical research or clinical documentation environment
• Sound knowledge of GCP, ICH, regulatory/clinical document requirements
• Proficiency with eTMF systems, Microsoft Office, Adobe Acrobat, and scanning tools

Desired Skills

• Strong interpersonal and communication skills
• Attention to detail and strong organizational skills
• Familiarity with electronic documentation systems
• Understanding of TMF processes and regulatory compliance

Work Location & Details

• Job Location: Bangalore, India
• Department: Clinical Operations / Clinical Documentation
• Last Date to Apply: June 28, 2025

Apply Here

Summary Table

Tagged as: Good Clinical Practice (GCP), Pharmaceutical Careers, Pharmaceutical Jobs