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Tmf Specialist Ii

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ICON
3+ years
Not Disclosed
Chennai, India
10 Feb. 19, 2026
Job Description
Job Type: Full Time Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

TMF Specialist II – Regulatory Document Management

Location: Chennai, India
Job Reference: JR142500
Company: ICON plc
Department: Regulatory Document Management (Office-Based Role)

Job Overview

ICON Strategic Solutions, a division of ICON plc, is hiring a TMF Specialist II to support Trial Master File (TMF) operations within a regulated clinical research environment. This role is critical to ensuring the accuracy, completeness, and compliance of essential clinical trial documentation in accordance with global regulatory standards and sponsor requirements.

The TMF Specialist II will contribute to client service projects and internal business operations by maintaining inspection-ready documentation aligned with ICH-GCP guidelines, regulatory authority expectations, and company SOPs.

This opportunity is ideal for clinical research professionals with experience in regulatory document management who are seeking career growth within a globally recognized CRO.

Key Responsibilities

  • Manage and maintain Trial Master File (TMF) documentation in compliance with ICH-GCP and regulatory standards

  • Ensure completeness, accuracy, and timely filing within electronic or paper TMF systems

  • Maintain audit and inspection readiness at all times

  • Support client service contracts and internal regulatory documentation activities

  • Perform quality control (QC) reviews of TMF documents

  • Collaborate with Clinical Operations, Regulatory Affairs, and Quality Assurance teams

  • Track TMF metrics and contribute to process improvements

  • Ensure adherence to client requirements and ICON Standard Operating Procedures

Required Experience

  • Minimum 3+ years of experience in clinical research, regulatory documentation, or Trial Master File management

  • Experience within a CRO, pharmaceutical, or biotechnology company preferred

  • Hands-on experience with eTMF systems and document management platforms

  • Strong understanding of ICH-GCP and global regulatory documentation standards

Educational Qualifications

  • Bachelor’s degree in Life Sciences, Pharmacy, Clinical Research, or a related discipline

Core Competencies

  • In-depth knowledge of TMF structure and regulatory documentation requirements

  • Strong attention to detail and organizational skills

  • Ability to manage multiple priorities within defined timelines

  • Effective communication and stakeholder coordination skills

  • Quality-driven approach with compliance-focused mindset

Why Join ICON?

ICON plc is a world-leading clinical research organization supporting pharmaceutical, biotechnology, and medical device companies across the full clinical development lifecycle.

Employees benefit from:

  • Competitive compensation structure

  • Comprehensive health insurance programs

  • Retirement and long-term savings plans

  • Annual leave entitlements

  • Global Employee Assistance Program (LifeWorks)

  • Life assurance coverage

  • Flexible country-specific benefits including wellness and family support programs

ICON is committed to diversity, inclusion, and equal employment opportunity, ensuring a professional environment that values performance, innovation, and career growth.