Looking for a career in clinical research and eTMF management? A new opportunity for a TMF Classifier I in Bangalore (Hybrid) has been posted, offering professionals with 6–12 months of clinical research experience a chance to work in a regulated environment aligned with GCP and ICH guidelines.

This role focuses on Trial Master File (TMF) management, document classification, and audit readiness—critical components in clinical trials. If you have a background in Life Sciences or Pharmacy, this is a high-growth entry point into the clinical operations domain.

Job Details

• Job Title: TMF Classifier I
• Location: Bangalore, India (Hybrid)
• Job Type: Full-Time
• Experience: 6–12 months
• Education: Bachelor’s in Life Sciences / Pharmacy / Business
• Last Date to Apply: April 29, 2026

Key Responsibilities – TMF Classifier I

• Manage document classification in Smart Inbox and ARC review
• Maintain electronic Trial Master Files (eTMF) across trial, country, and site levels
• Perform audit-ready checks ensuring document accuracy and compliance
• Conduct visual quality checks for document clarity and completeness
• Handle document deletion and lifecycle tracking
• Ensure compliance with GCP, ICH guidelines, and SOPs
• Support internal and sponsor audits, including corrective actions
• Collaborate with study teams and stakeholders for TMF quality
• Identify and resolve operational TMF issues
• Participate in process improvement initiatives

Required Qualifications

• Bachelor’s degree in Life Sciences / Pharmacy / Business
• 6–12 months experience in clinical research or eTMF management
• Strong understanding of:
  • GCP (Good Clinical Practice)
  • ICH guidelines
  • Clinical/regulatory documentation
• Proficiency in:
  • Microsoft Office
  • Adobe Acrobat
  • Web-based clinical systems

Preferred Qualifications

• Master’s degree in Life Sciences or related field
• Experience with electronic clinical systems (eTMF platforms)
• Exposure to clinical trial documentation workflows

Salary & Benefits

• Estimated Salary: ₹3.2 LPA – ₹5.5 LPA
• Hybrid working model
• Exposure to global clinical trials and audits
• Career growth in clinical operations & regulatory domain
• Opportunity to work with cross-functional study teams

Why This Role is Valuable

The TMF Classifier I role is a foundational position in clinical research, providing hands-on experience in:

• Trial Master File (TMF) systems
• Regulatory compliance
• Audit readiness processes

This experience is highly valuable for advancing into roles like:

• Clinical Trial Associate (CTA)
• Clinical Operations Specialist
• Regulatory Affairs Associate

How to Apply

Application Link