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Sr. Tmf Reviewer

Fortrea
8-10 years
INR 12 LPA – 18 LPA
Bangalore, India
1 June 17, 2026
Job Description
Job Type: Full Time Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences Skills: ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing

Sr. TMF Reviewer

Location: Bangalore
Employment Type: Full Time


Job Overview

The Sr. TMF Reviewer is responsible for managing ARC reviews and performing comprehensive Trial Master File (TMF) reviews of electronic Trial Master Files (eTMF), including Trial, Country, and Site-level artifacts for clinical studies. The role ensures TMF quality, completeness, compliance, and audit readiness in accordance with regulatory requirements, sponsor expectations, GCP, and ICH guidelines.


Summary of Responsibilities

  • Provide process oversight, control, coordination, and approval of clinical trial documentation.

  • Manage and review electronic Trial Master Files (eTMF) across Phase I-IV clinical studies.

  • Maintain a thorough understanding of applicable regulatory requirements and TMF standards.

  • Manage Trial, Country, and Site artifacts within the eTMF system.

  • Collaborate with Study Team Members and key stakeholders to ensure TMF completeness and compliance.

  • Perform detailed TMF reviews and quality checks on study documentation.

  • Participate in centralized TMF review activities and coordinate with Project Teams and Quality Control groups.

  • Map Sponsor TMF Indexes against Fortrea Universal Content Vocabulary (UCV) and TMF structures where applicable.

  • Maintain TMFs in a continuous state of audit readiness.

  • Perform Audit Ready Checks on uploaded documents to ensure accuracy, completeness, and contextual relevance.

  • Initiate and manage "What's Missing" activities to identify and obtain incomplete, inaccurate, or missing artifacts.

  • Track document completeness against TMF Plans, TMF Indexes, and study milestones.

  • Ensure compliance with established TMF review performance metrics.

  • Process, track, and maintain final essential documents throughout all study phases.

  • Ensure compliance with:

    • Fortrea SOPs

    • Sponsor SOPs

    • ICH Guidelines

    • Good Clinical Practice (GCP)

  • Identify and resolve operational issues related to TMF management.

  • Support study teams with data collection and status reporting activities.

  • Prepare TMFs for sponsor audits, QA audits, and regulatory inspections.

  • Support audit finding resolution and implementation of corrective actions.

  • Participate in client audits and regulatory inspections.

  • Review TMF quality issues, identify trends, and escalate risks or concerns to management.

  • Collaborate with internal stakeholders to improve TMF quality and compliance.

  • Ensure high levels of client satisfaction across assigned studies.

  • Participate in business process improvement and continuous quality initiatives.

  • Attend internal and external study team meetings as required.

  • Complete assigned training and development activities.

  • Interact directly with clients when required.

  • Perform additional duties as assigned.


Qualifications (Minimum Required)

  • Bachelor's Degree in Life Sciences, Business Administration, or a related discipline.

  • Equivalent experience may be considered in lieu of formal educational qualifications.

  • Strong interpersonal and communication skills.


Experience (Minimum Required)

  • 8 to 10 years of experience in a Clinical Research environment.

  • Strong understanding of:

    • Good Clinical Practice (GCP)

    • International Council for Harmonisation (ICH) Guidelines

    • Regulatory Documentation Requirements

    • Clinical Trial Documentation Processes

  • Experience managing and reviewing electronic Trial Master Files (eTMF).

  • Knowledge of:

    • Microsoft Office Suite

    • Adobe Acrobat Standard

    • Web-Based Clinical Systems

    • Document Management Platforms

    • Scanning and Document Processing Software

  • Experience preparing documentation for audits and inspections.

  • Strong attention to detail and quality compliance.


Preferred Qualifications

  • Master's Degree in Life Sciences, Business Administration, or a related field.

  • Extensive experience within clinical research and TMF management environments.

  • Experience working with:

    • eTMF Systems

    • Clinical Trial Management Systems (CTMS)

    • Electronic Clinical Systems

  • Experience supporting global clinical trials.