IQVIA Hiring TMF Specialist | Clinical Trials Documentation Job in Bangalore

Mohit March 18, 2026

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IQVIA Hiring TMF Specialist | Clinical Trials Documentation Job in Bangalore

✔ Verified by Medical Jobs India

TMF Specialist | Clinical Trials Documentation Role

IQVIA

Bangalore

3 Years

Clinical Trials

TMF

🏢 About IQVIA

IQVIA is a global leader in clinical research, healthcare analytics, and life sciences consulting. The company supports pharmaceutical and biotech organizations through advanced data, clinical trials, and regulatory solutions.

📌 Job Overview

Role: TMF Specialist
Company: IQVIA
Location: Bangalore, India
Experience: 3 Years
Department: Clinical Trials / Records Management

🔬 Key Responsibilities

Maintain Trial Master File (TMF) compliance
Ensure document accuracy and completeness
Coordinate records retrieval and storage
Manage document lifecycle (storage, archive, disposal)
Support clinical teams with document access
Prepare studies for archival transfer
Train teams on TMF processes

🎓 Eligibility Criteria

B.Pharm / M.Pharm / Pharm.D
BSc / MSc Life Sciences
Related healthcare field

Experience Required:

Minimum 3 years in TMF / Records Management
Experience in clinical documentation

💻 Required Skills

ICH-GCP knowledge
TMF structure understanding
Regulatory compliance
Documentation and audit readiness
Strong communication skills

⭐ Benefits of Working at IQVIA

Global clinical trial exposure
Career growth in TMF & regulatory documentation
Work with global project teams
Strong learning environment

🎯 Interview Preparation Tips

Understand TMF structure & sections
Learn ICH-GCP guidelines
Know document lifecycle (creation → archive)
Prepare audit & inspection readiness concepts

Helpful resources:

📌 Note Before You Apply:
Kindly read the entire job description carefully before applying. Make sure your experience aligns with TMF and clinical documentation requirements.