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If you have solid experience in clinical research and are looking to advance your career, here’s a strong opportunity with a global CRO.

Fortrea is hiring for the position of TMF Reviewer II in Bangalore. This role is ideal for professionals experienced in Trial Master File (TMF) management and clinical documentation within regulated environments.

About Fortrea

Fortrea is a global clinical research organization known for delivering high-quality clinical development solutions. The company works closely with pharmaceutical and biotech organizations to support clinical trials across all phases.

With a strong focus on compliance, innovation, and patient outcomes, Fortrea offers a professional and collaborative environment for career growth.

Job Overview

Company: Fortrea
Role: TMF Reviewer II
Location: Bangalore, India
Experience: 6 to 10 Years
Qualification: Bachelor’s in Life Sciences/Business (Master’s preferred)
Work Type: Full-time (Office-based)

Role Summary

As a TMF Reviewer II, you will be responsible for reviewing and maintaining electronic Trial Master Files (eTMF) to ensure completeness, accuracy, and audit readiness.

This role plays a key part in supporting clinical trials by ensuring all documentation meets regulatory standards.

Skills Required

Strong understanding of GCP and ICH guidelines
Knowledge of clinical and regulatory documentation
Experience with eTMF systems
Proficiency in MS Office and document tools
Excellent attention to detail
Strong communication and coordination skills
Ability to manage audit-ready documentation

Key Responsibilities

Review and manage eTMF documents
Ensure completeness of Trial, Country, and Site files
Perform QC checks and audit readiness reviews
Track missing or incomplete documents
Support sponsor and internal audits
Maintain compliance with TMF plans and indexes
Collaborate with study teams
Identify and resolve documentation issues
Support continuous improvement initiatives

Benefits & Career Growth

Work with a global clinical research organization
Exposure to Phase I–IV clinical trials
Career growth in TMF and clinical operations
Learning and development opportunities
Collaborative and professional work culture
Long-term stability in clinical research

Why You Should Apply

Fortrea offers a platform where your expertise in TMF and clinical documentation directly contributes to successful clinical trials. You’ll work in a structured environment that values quality, compliance, and continuous improvement.

How to Apply

Apply through the official Fortrea careers portal using:
Job Requisition ID: 263735

Verification: To confirm the legitimacy of this posting, you can view the original announcement on the Fortrea career page.

Last Date to Apply: 7 August 2026

APPLY FOR THIS JOB

Ensure your resume highlights:

TMF and clinical research experience
Knowledge of GCP/ICH guidelines
Experience with eTMF systems

FAQs

1. Who is eligible for this role?

Candidates with a Bachelor’s degree in Life Sciences or Business and 6–10 years of clinical research experience are eligible.

2. Is this a remote job?

No, this is a full-time office-based role in Bangalore.

3. What skills are most important?

Strong knowledge of TMF processes, GCP/ICH guidelines, and attention to detail are essential.

4. What is the last date to apply?

The application deadline is 7 August 2026.

5. What career growth can I expect?

You can progress into senior TMF roles, clinical operations, or quality management positions.

Link this article to:

Fortrea Hiring TMF Reviewer II in Bangalore | Clinical Research Jobs 2026 (6–10 Years Experience)