Fortrea Hiring TMF Classifier I, Clinical Research

Fortrea Hiring TMF Classifier I in Bangalore | Clinical Research eTMF Jobs

Clinical research professionals searching for TMF and eTMF jobs in Bangalore now have an excellent opportunity with Fortrea. The company is currently hiring candidates for the role of TMF Classifier I for its hybrid clinical research operations team. This full-time opportunity is ideal for candidates with experience in Trial Master File management, clinical documentation review, regulatory compliance, GCP guidelines, and clinical research operations.

As pharmaceutical and CRO companies continue expanding global clinical trials, healthcare compliance systems, and regulatory documentation management, the demand for professionals with expertise in electronic Trial Master File (eTMF) operations is increasing rapidly across India. Fortrea is actively strengthening its clinical trial documentation and TMF management functions to support regulatory compliance, audit readiness, and high-quality clinical research operations.

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Company Overview

Fortrea is a globally recognized Contract Research Organization (CRO) specializing in clinical development, healthcare research, regulatory support, and clinical trial management services.

The company supports pharmaceutical, biotechnology, and medical device organizations by providing clinical trial solutions, healthcare analytics, patient-focused research services, and regulatory compliance support. Fortrea works across multiple therapeutic areas and helps global healthcare organizations accelerate drug development and improve patient outcomes.

Fortrea’s clinical operations and TMF management teams focus on maintaining high-quality regulatory documentation, audit-ready clinical trial systems, healthcare compliance standards, and efficient clinical research workflows.

Employees gain exposure to global clinical trials, electronic Trial Master File systems, healthcare documentation standards, and international regulatory requirements while working within collaborative and process-driven project environments.

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Job Role & Responsibilities

Fortrea is hiring candidates for the role of TMF Classifier I to support eTMF management, clinical trial document classification, audit readiness activities, and healthcare compliance operations.

This clinical research and eTMF role requires strong understanding of GCP guidelines, clinical documentation management, regulatory compliance standards, and audit-ready TMF maintenance.

Key Responsibilities

• Manage document classification activities under Smart Inbox and ARC review processes
• Support document deletion and TMF maintenance activities
• Maintain electronic Trial Master Files (eTMF) including Trial, Country, and Site artifacts
• Collaborate with Study Team Members and Start-Up teams for TMF operations
• Perform visual quality checks of electronic documents before release
• Ensure image clarity, readability, and document accuracy within eTMF systems
• Conduct Audit Ready Checks for uploaded clinical trial documents
• Process and track essential clinical trial artifacts throughout all study phases
• Ensure compliance with company SOPs, sponsor SOPs, GCP, and ICH guidelines
• Identify operational issues related to TMF processes and support resolution activities
• Prepare TMF documentation for QA audits and sponsor inspections
• Participate in internal and client audit activities when required
• Support business improvement initiatives related to quality and productivity
• Attend internal and external study meetings as needed
• Maintain audit-ready documentation and regulatory compliance throughout study lifecycle

Preferred Technical Skills

Candidates applying for this clinical research and eTMF role should have practical knowledge in:

• Electronic Trial Master File (eTMF) systems
• Clinical trial documentation
• Regulatory compliance
• GCP guidelines
• ICH standards
• TMF classification
• Audit readiness
• Clinical operations
• Healthcare documentation management
• Regulatory document review
• Quality assurance systems
• Clinical research workflows
• SOP compliance
• Microsoft Office applications
• Adobe Acrobat and document management tools

Candidates with prior experience in CRO operations, healthcare compliance systems, clinical documentation review, and electronic clinical systems will have an added advantage.

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Eligibility / Qualifications

Candidates interested in this TMF Classifier I vacancy should meet the following eligibility criteria.

Educational Qualification

Applicants should possess a Bachelor’s Degree in Life Sciences or Business-related disciplines.

Eligible educational qualifications include:

B.Pharm, M.Pharm, BSc, MSc, Biotechnology, Clinical Research, Life Sciences, Biochemistry, Microbiology, Biomedical Sciences, Pharmaceutical Sciences, Healthcare Management, Nursing, Medical Laboratory Sciences, Business Administration, or related healthcare and life science disciplines.

Candidates with Master’s Degree qualifications in Life Sciences or Business-related fields will have an advantage.

Experience Required

• Minimum 6 months to 12 months of experience in a clinical research environment
• Knowledge of GCP and ICH guidelines required
• Prior experience with clinical electronic systems preferred
• Understanding of regulatory and clinical document requirements beneficial

Essential Skills

• Strong attention to detail and documentation skills
• Good understanding of healthcare compliance and clinical research processes
• Excellent interpersonal and communication abilities
• Ability to work within cross-functional clinical research teams
• Familiarity with Microsoft Office products and Adobe Acrobat
• Knowledge of document scanning and web-based applications
• Strong organizational and audit preparation skills
• Ability to maintain high-quality clinical trial documentation

Professionals interested in clinical research careers, eTMF jobs, healthcare documentation roles, CRO operations, and regulatory compliance opportunities are encouraged to apply.

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Location & Salary

Job Location

Bangalore

Salary

Based on current CRO and clinical research market trends in Bangalore, the expected salary for the TMF Classifier I role may range approximately between ₹3.5 LPA to ₹5.5 LPA depending on candidate experience, technical expertise, and interview performance.

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Application Process

Interested and eligible candidates can apply online through the official Fortrea careers portal.

Apply Here: https://fortrea.wd1.myworkdayjobs.com/Fortrea/job/Bangalore/TMF-Classifier-I_262480

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Frequently Asked Questions (FAQs)

1. What is the role offered by Fortrea?

Fortrea is hiring candidates for the position of TMF Classifier I in Bangalore.

2. What qualifications are eligible for this eTMF job?

Candidates with B.Pharm, M.Pharm, BSc, MSc, Biotechnology, Clinical Research, Life Sciences, and related healthcare qualifications can apply.

3. How much experience is required for this role?

Applicants should have 6 months to 12 months of experience working in a clinical research environment.

4. What skills are important for this position?

eTMF management, clinical documentation review, GCP compliance, audit readiness, healthcare documentation, and regulatory compliance skills are important for this role.

5. Is this a remote or hybrid role?

This position follows a hybrid work model.

6. What is the expected salary for this role?

The expected salary may range approximately between ₹3.5 LPA to ₹5.5 LPA depending on candidate experience and technical expertise.

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Summary Table

Category	Details
Company	Fortrea
Department Vacancies	TMF Classifier I, Clinical Research
Qualification	B.Pharm, M.Pharm, BSc, MSc, Biotechnology, Clinical Research, Life Sciences
Experience	6 Months – 1 Year
Location	Bangalore

Tagged as: Pharma Jobs in Bangalore