TMF Classifier I Job at Fortrea Entry Level Clinical Research for clinical research professionals with eTMF and GCP knowledge.
Job Title: TMF Classifier I
Company: Fortrea
Location: Bangalore, India (Hybrid)
Job Type: Full-Time
Experience Required: 6–12 Months
Education: B.Pharm, M.Pharm, Pharm.D, M.Sc, B.Sc (Life Sciences), MBA
Job Status: Verified Job
Application Mode: Online Application
Fortrea, a leading global Contract Research Organization (CRO), is hiring TMF Classifier I professionals for its Bangalore location in a hybrid work model. This role is ideal for candidates seeking an entry-level clinical research career with hands-on exposure to electronic Trial Master File (eTMF) management, regulatory compliance, and audit readiness. TMF Classifier I Job at Fortrea
About the Company
Fortrea is a globally recognized CRO dedicated to advancing healthcare through innovative and high-quality clinical research. With a strong focus on compliance, collaboration, and patient safety, Fortrea supports clinical trials across multiple therapeutic areas and regions. The organization offers a professional, inclusive, and growth-oriented environment for early-career and experienced clinical research professionals. TMF Classifier I Job at Fortrea
Job Details
- Job Title: TMF Classifier I
- Company Name: Fortrea
- Employment Type: Full-Time
- Work Model: Hybrid
- Job Location: Bangalore, India
- Experience Level: 6–12 months
- Functional Area: Clinical Operations / TMF Management
- Industry: Clinical Research / CRO
Job Description
As a TMF Classifier I, you will support the management and maintenance of electronic Trial Master Files (eTMF) for clinical studies. The role ensures TMF completeness, quality, and compliance with regulatory requirements throughout all phases of clinical trials. You will collaborate closely with study teams, startup teams, and business process groups to maintain audit-ready TMFs and support inspections. TMF Classifier I Job at Fortrea
Key Responsibilities
- Manage electronic Trial Master Files including Trial, Country, and Site-level artifacts
- Perform document classification under Smart Inbox and conduct ARC reviews
- Manage document deletion activities as per TMF processes
- Conduct visual quality checks to ensure document clarity and readability
- Perform Audit Ready Checks to confirm document accuracy and correct context
- Track and process essential TMF documents across all study phases
- Ensure compliance with company SOPs, sponsor SOPs, GCP, and ICH guidelines
- Identify TMF-related operational issues and support resolution activities
- Prepare TMF for QA and sponsor audits and implement corrective actions
- Participate in internal audits and client audits as required
- Collaborate with study teams and business process teams
- Attend internal and external study team meetings when required
- Support continuous improvement initiatives to enhance quality and productivity
TMF Classifier I Job at Fortrea
Skills / Qualifications
Minimum Required
- Bachelor’s degree in Life Sciences or Business
- 6–12 months of experience in a clinical research environment
- Clear understanding of ICH-GCP guidelines
- Knowledge of regulatory and clinical document requirements
- Proficiency in Microsoft Office and web-based applications
- Working knowledge of Adobe Acrobat Standard and document scanning tools
- Strong interpersonal and communication skills
- High attention to detail and compliance
TMF Classifier I Job at Fortrea
Preferred Qualifications
- Master’s degree in Life Sciences or Business
- Experience working with clinical electronic systems
- Equivalent clinical research experience may be considered in place of formal education
TMF Classifier I Job at Fortrea
Benefits / Perks
- Hybrid work model offering flexibility and work-life balance
- Structured learning and career development in clinical research
- Exposure to global clinical trials and regulatory environments
- Supportive and collaborative team culture
- Minimal travel requirement (less than 10%)
TMF Classifier I Job at Fortrea
Why You Should Join
This role is a strong starting point for building a long-term career in clinical research and TMF management. At Fortrea, you will gain valuable exposure to global trials, regulatory standards, and audit processes while working in a supportive, growth-focused environment that values teamwork and quality. TMF Classifier I Job at Fortrea
How to Apply
Interested candidates should apply through the official Fortrea career portal using the provided online application link. Ensure your resume highlights relevant clinical research experience, TMF exposure, and knowledge of GCP and ICH guidelines.
FAQs
Is this role suitable for freshers?
Candidates should have at least 6 months of experience in a clinical research environment.
Is the job fully remote?
No, this is a hybrid role based in Bangalore.
What systems will I work on?
You will work on electronic Trial Master File (eTMF) systems, Smart Inbox, and clinical document management tools.
Does this role involve audits?
Yes, the role supports audit readiness, internal audits, and sponsor audits.
For verified pharma job updates, visit PharmaJobHub.in – India’s trusted pharma career portal.
Note: This job information is sourced from publicly available official sources. We share it for reference purposes only and do not claim ownership of the job posting.
