Apply for TMF Classifier II job at Fortrea Bangalore. Check eligibility, salary, experience, clinical research role details and apply online now.
The TMF Classifier Jobs at Fortrea 2026 offer an excellent opportunity for candidates looking to build a career in clinical research documentation and Trial Master File (TMF) management. This hybrid role in Bangalore is ideal for professionals with 1–2 years of experience in eTMF systems, GCP compliance, and clinical operations. If you are aiming to grow in the CRO industry, this role provides strong exposure to global clinical trials and regulatory processes.
Job Overview
| Field | Details |
|---|---|
| Job Title | TMF Classifier II |
| Company Name | Fortrea |
| Location | Bangalore, Karnataka |
| Employment Type | Full-Time |
| Department | Clinical Operations / TMF Management |
| Experience Required | 1–2 Years |
| Education | B.Pharm, M.Pharm, Pharm.D, B.Sc, M.Sc, Life Sciences / Business |
| Salary | ₹4.5 LPA – ₹7 LPA (Estimated) |
Company Overview
Fortrea is a leading global Contract Research Organization (CRO) that provides clinical development and commercialization services to pharmaceutical and biotechnology companies. The company focuses on delivering high-quality clinical trials, regulatory support, and innovative solutions, making it a strong platform for career growth in clinical research.
Job Location & Employment Type
- Location: Bangalore, Karnataka
- Work Mode: Hybrid
- Employment Type: Full-Time
Open Positions / Department Details
TMF Classifier II – Clinical Documentation Role
This position focuses on managing electronic Trial Master Files (eTMF) and ensuring compliance with global regulatory standards throughout the clinical trial lifecycle.
Key Roles & Responsibilities
eTMF Management & Classification
- Manage Trial, Country, and Site-level TMF documents
- Perform document classification using Smart Inbox and ARC review systems
- Handle document lifecycle including deletion and updates
Audit Readiness & Quality Control
- Conduct quality checks for document clarity and readability
- Ensure TMF is audit-ready at all times
- Perform audit readiness checks for accuracy and completeness
Compliance & Documentation
- Ensure adherence to ICH-GCP guidelines and SOPs
- Track and manage essential clinical trial documents
- Maintain regulatory compliance across all study phases
Issue Resolution & Collaboration
- Identify and resolve TMF-related operational issues
- Collaborate with study teams, clinical operations, and sponsors
Audit & Inspection Support
- Prepare TMF for QA and sponsor audits
- Support CAPA (Corrective and Preventive Actions) implementation
Continuous Improvement
- Participate in process improvement initiatives
- Support training and mentoring activities
Eligibility Criteria
Education
- Bachelor’s Degree in Life Sciences or Business
- B.Pharm, M.Pharm, Pharm.D, B.Sc, M.Sc candidates eligible
- Master’s Degree (Preferred)
Experience
- 1–2 years of experience in clinical research or eTMF
Skills Required
- Strong knowledge of ICH-GCP guidelines
- Understanding of clinical regulatory documents
- Experience with eTMF systems (e.g., Veeva Vault preferred)
- Proficiency in Microsoft Office and Adobe Acrobat
- Good communication and interpersonal skills
- Attention to detail and organizational ability
Salary & Benefits
- Salary: ₹4.5 LPA – ₹7 LPA (Estimated)
- Hybrid work flexibility
- Exposure to global clinical trials
- Career growth in TMF and clinical operations
- Opportunity to work with international sponsors
- Learning and development opportunities
Selection Process
The recruitment process generally includes:
- Resume screening
- Technical interview
- HR interview
- Final selection
How to Apply
Interested candidates can apply online through the official Fortrea careers portal.
Ensure your resume highlights:
- Experience in eTMF or clinical documentation
- Knowledge of GCP guidelines
- Relevant technical skills
Why Apply for This Job?
The TMF Classifier Jobs at Fortrea 2026 offer strong career advantages:
- Work with a global CRO in clinical research
- Gain expertise in TMF and regulatory compliance
- Exposure to international clinical trial standards
- Hybrid work environment
- Strong career progression in clinical operations
This role is ideal for professionals aiming to specialize in clinical documentation and regulatory processes.
FAQs
1. Who can apply for TMF Classifier II at Fortrea?
Candidates with Life Sciences or Pharmacy background and 1–2 years experience can apply.
2. What is the salary offered?
The estimated salary ranges from ₹4.5 LPA to ₹7 LPA.
3. Is this a work-from-home job?
It is a hybrid role based in Bangalore.
4. What skills are required?
Knowledge of GCP, eTMF systems, and clinical documentation is essential.
5. How can I apply?
You can apply through the official careers portal of Fortrea.
Conclusion
The TMF Classifier Jobs at Fortrea 2026 are a great opportunity for candidates with clinical research experience to advance their careers in TMF management and regulatory compliance. With global exposure, structured processes, and growth potential, this role is ideal for building a strong foundation in the CRO industry. Apply now to take the next step in your career.
Disclaimer
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