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Tmf Reviewer Ii

Fortrea
6-10 years
Not Disclosed
Bangalore, India
10 June 3, 2026
Job Description
Job Type: Full Time, Hybrid, Remote Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Clinical Trials, Detail-Oriented, Drug Development, Lifesciences, Negotiation Skills, Regulatory Compliance, Communication Skills, CPC Certified, Data Analysis, Document Management, Life Science, Regulatory Compliance, Waterfall Model, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, mRS and EQ-5D-5L, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

TMF Reviewer II

Location: Bangalore
Category: Clinical
Job ID: 262543


Role Overview

The TMF Reviewer II is responsible for the review, quality control, and maintenance of electronic Trial Master Files (eTMF) for clinical studies. The role ensures that trial documentation across trial, country, and site levels is complete, accurate, and audit-ready in compliance with regulatory requirements, sponsor expectations, and company SOPs.

This position plays a key role in maintaining inspection readiness and supporting clinical study documentation integrity across all phases of clinical trials (Phase I–IV).


Key Responsibilities

1. eTMF Management & Review

  • Perform review of electronic Trial Master Files (eTMF).

  • Manage trial, country, and site-level artifacts for clinical studies.

  • Ensure proper classification and indexing of TMF documents.

  • Maintain TMF structure aligned with sponsor and internal requirements.


2. Quality Control & Compliance

  • Perform audit-ready checks on all uploaded documents.

  • Ensure completeness, accuracy, and context correctness of TMF documents.

  • Identify missing, incomplete, or incorrect documents and track resolution.

  • Ensure compliance with:

    • GCP (Good Clinical Practice)

    • ICH guidelines

    • Sponsor SOPs

    • Internal Fortrea SOPs


3. TMF Maintenance & Tracking

  • Maintain TMF in an audit-ready state across all study phases.

  • Track essential documents throughout the clinical trial lifecycle.

  • Initiate “What’s Missing” tracking for incomplete TMF content.

  • Ensure alignment with TMF plans, indices, and study milestones.


4. Document Mapping & System Management

  • Map sponsor TMF index with internal systems (UCV, TMF tools).

  • Perform QC checks in sponsor systems (e.g., TMF Classifier where applicable).

  • Ensure accurate document classification in electronic systems.


5. Audit & Inspection Support

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

  • Support audit responses and corrective action implementation.

  • Participate in client audits and inspections when required.


6. Issue Management & Reporting

  • Identify operational issues related to TMF processes.

  • Track and resolve TMF-related documentation gaps.

  • Report trends and recurring issues to management.

  • Support study teams with TMF status reporting and data requests.


7. Cross-Functional Collaboration

  • Work closely with:

    • Study teams

    • Project team members

    • Quality Control teams

    • Global study stakeholders

  • Ensure effective communication and coordination across teams.


8. Process Improvement

  • Participate in initiatives to improve TMF quality and efficiency.

  • Contribute to continuous improvement of TMF processes and workflows.

  • Identify trends and recommend corrective and preventive actions.


9. Meetings & Communication

  • Attend internal and external study team meetings as required.

  • Provide updates on TMF status and documentation quality.

  • Support client satisfaction through timely and accurate reporting.


Required Qualifications

Education

  • Bachelor’s degree in:

    • Life Sciences

    • Business

    • Related field

  • Or equivalent experience in clinical research


Experience

  • 6–10 years of experience in clinical research environment

  • Strong knowledge of:

    • Clinical trial documentation

    • TMF processes

    • Regulatory requirements


Technical Knowledge

  • Strong understanding of:

    • GCP (Good Clinical Practice)

    • ICH guidelines

    • Clinical documentation requirements

  • Proficiency in:

    • Microsoft Office Suite

    • Web-based systems

    • Adobe Acrobat

    • eTMF systems


Skills & Competencies

  • Strong attention to detail and quality focus

  • Excellent communication and interpersonal skills

  • Ability to manage documentation-heavy processes

  • Strong organizational and tracking abilities

  • Ability to work in a structured, compliance-driven environment

  • Strong analytical and problem-solving skills


Preferred Qualifications

  • Master’s degree in Life Sciences or Business-related field

  • Experience with electronic clinical systems (eTMF platforms)

  • Strong familiarity with clinical research documentation workflows


Work Environment

  • Office-based work environment

  • Minimal travel (<10%), mainly for:

    • Sponsor meetings

    • Client meetings

    • Internal Fortrea locations