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Tmf Reviewer Ii

Fortrea
6+ years
₹8,00,000 – ₹18,00,000 per annum
Bangalore, India
15 June 24, 2026
Job Description
Job Type: Full Time, Hybrid Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: Regulatory Affairs, Regulatory Writing, Regulatory Compliance, Global Submissions, eCTD, IND/NDA/BLA Submissions, ICH-GCP, Regulatory Strategy, Regulatory Intelligence, Labeling Strategy.

Job Title
TMF Reviewer II

Company
Fortrea

Location
Bangalore, India

Job Overview
The TMF Reviewer II is responsible for managing, reviewing, and ensuring the completeness and audit readiness of electronic Trial Master Files (eTMF) for clinical studies across Phases I–IV. The role ensures compliance with regulatory requirements and supports clinical trial documentation quality, inspection readiness, and sponsor satisfaction.


Key Responsibilities

1. eTMF Management & Document Review

  • Perform review of electronic Trial Master Files (eTMF) across trial, country, and site levels

  • Ensure proper classification, indexing, and mapping of TMF documents

  • Conduct quality control checks on uploaded study documents

  • Maintain audit-ready status of TMF systems across all study phases


2. Quality & Compliance Oversight

  • Ensure compliance with GCP, ICH guidelines, and sponsor SOPs

  • Perform audit-ready checks on all essential clinical trial documents

  • Identify missing, incomplete, or incorrect artifacts and track resolution

  • Maintain TMF completeness in alignment with TMF plans and indexes


3. Audit & Inspection Support

  • Prepare TMF for sponsor and regulatory audits

  • Support responses and corrective actions for audit findings

  • Participate in regulatory inspections and client audits

  • Ensure continuous inspection readiness of all TMF documentation


4. Issue Management & Reporting

  • Identify operational issues related to TMF and support resolution

  • Track TMF performance metrics and compliance indicators

  • Report trends in document quality issues to management

  • Support study teams with TMF-related status reporting


5. Cross-functional Collaboration

  • Work closely with study teams, quality teams, and sponsors

  • Attend study meetings as required

  • Collaborate with global teams to ensure documentation consistency

  • Support client satisfaction through high-quality TMF management


6. Process Improvement

  • Participate in business improvement and quality enhancement initiatives

  • Contribute to continuous improvement of TMF processes and workflows

  • Support standardization of documentation practices across studies


Required Qualifications

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

  • 6–10 years of experience in clinical research environment

  • Strong understanding of GCP and ICH guidelines

  • Knowledge of clinical trial documentation and regulatory requirements

  • Proficiency in MS Office and Adobe Acrobat

  • Experience working with electronic clinical systems (preferred)

  • Strong attention to detail and documentation accuracy

  • Good communication and interpersonal skills


Preferred Qualifications

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

  • Experience with eTMF systems

  • Exposure to audits and regulatory inspections

  • Experience in CRO or sponsor-side clinical operations


Work Environment

  • Office-based role (Bangalore)

  • Minimal travel (<10%) for audits or client meetings