Fortrea Hiring TMF Classifier II | Clinical Document Management Job
Fortrea is hiring TMF Classifier II professionals for its clinical operations and Trial Master File (TMF) management team in Bangalore.
This opportunity is ideal for candidates interested in Clinical Document Management, eTMF Operations, Trial Master File Management, Audit Readiness, GCP Compliance, and Clinical Operations careers.
📋 Fortrea Hiring Overview
- Company: Fortrea
- Role: TMF Classifier II
- Location: Bangalore
- Work Mode: Hybrid
- Industry: Clinical Research
- Department: Clinical Operations / TMF
- Experience: 1–2 Years
- Last Date: 24 May 2026
🏢 About Fortrea
Fortrea is a leading global clinical research organization (CRO) providing clinical development, patient access, and technology solutions to pharmaceutical, biotechnology, and medical device companies worldwide.
The organization supports global clinical trials and regulatory operations through advanced clinical systems, TMF management, and compliance-driven processes.
📌 Key Responsibilities
📂 eTMF Management & Classification
- Manage Trial, Country, and Site artifacts within eTMF systems
- Perform document classification and ARC reviews
- Handle document deletion and lifecycle management activities
✅ Audit Readiness & Quality Control
- Conduct document quality and readability checks
- Perform Audit Ready Checks for TMF completeness
- Maintain continuous audit readiness standards
📊 Compliance & Documentation
- Ensure compliance with ICH-GCP guidelines
- Follow sponsor SOPs and company procedures
- Track and manage essential clinical documents
🔧 Collaboration & Issue Resolution
- Identify and resolve TMF operational issues
- Collaborate with study teams and sponsors
- Support process improvement initiatives
📑 Audit & Inspection Support
- Prepare TMF for QA and sponsor audits
- Support CAPA implementation activities
- Assist during inspections and compliance reviews
🎓 Eligibility Criteria
Eligible Qualifications
- B.Pharm / M.Pharm / Pharm.D
- BSc / MSc Life Sciences
- Business Graduates
- Healthcare & Clinical Research Related Degrees
🧑💻 Experience Required
- 1–2 Years Experience in Clinical Research
- Experience in eTMF or Document Management
- Clinical Operations or Regulatory Documentation Exposure
⭐ Required Skills
- Knowledge of ICH-GCP guidelines
- Understanding of clinical regulatory documents
- Experience with eTMF systems
- MS Office & Adobe Acrobat proficiency
- Communication and collaboration skills
- Attention to detail and compliance mindset
🌍 Benefits of Working at Fortrea
- Hybrid work flexibility
- Exposure to global clinical trials
- Career growth in TMF & Clinical Operations
- Hands-on experience in audit readiness
- Global sponsor interaction opportunities
- Collaborative work environment
🚀 Why This Role is Valuable
This TMF Classifier II role provides excellent opportunities to build expertise in:
- Trial Master File (TMF) Management
- Clinical Document Management
- eTMF Systems & Compliance
- Audit Readiness & CAPA
- Clinical Operations
- Regulatory Documentation
Candidates will gain exposure to global clinical documentation workflows, sponsor audits, and regulatory compliance systems.
📄 Resume & Interview Tips
- Highlight TMF or clinical documentation experience clearly
- Mention eTMF systems exposure if available
- Showcase GCP and audit readiness knowledge
- Add regulatory or sponsor coordination experience
- Keep resume ATS-friendly and concise
🚀 Job Application Link
Please make sure to read the complete job description carefully before submitting your application. Understanding TMF workflows, audit readiness, eTMF systems, and GCP compliance improves your chances of selection and creates a strong professional impression.
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