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Tmf Specialist

IQVIA
1-15 years
Not Disclosed
Bangalore, Chennai, India
1 June 9, 2026
Job Description
Job Type: Hybrid Education: M.Pharm/B.Pharm or M.Sc. Skills: MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, mRS and EQ-5D-5L.

TMF Specialist (All Levels)

Locations: Chennai, India | Bangalore, India
Work Model: Hybrid (Office with Flex)
Job Type: Full-Time
Job Requisition ID: JR142623


About ICON

ICON is a global healthcare intelligence and clinical research organization dedicated to accelerating the development of innovative medicines and treatments that improve patient lives worldwide.

Driven by our core values of Integrity, Collaboration, Agility, and Inclusion, we foster a culture that supports professional growth, innovation, and meaningful contributions to global healthcare.


About the Role

We are seeking experienced TMF Specialists (Trial Master File Specialists) across multiple experience levels to support clinical trial document management activities for global studies.

In this role, you will be responsible for maintaining Trial Master Files (TMF), processing study documentation, ensuring compliance with regulatory requirements, supporting audit readiness, and collaborating with study teams and clients throughout the clinical trial lifecycle.

This opportunity is ideal for professionals with strong TMF expertise and a solid understanding of clinical trial documentation and regulatory requirements.


Key Responsibilities

Trial Master File (TMF) Management

  • Maintain and manage Trial Master Files (TMF) in accordance with:

    • Study-specific requirements

    • Client requirements

    • Company SOPs and Work Practices (WPs)

    • Regulatory guidelines

  • Ensure TMF completeness, accuracy, and inspection readiness throughout the study lifecycle.

  • Support ongoing maintenance and reconciliation activities.

Clinical Document Processing

  • Process clinical study documents according to established procedures.

  • Perform activities including:

    • Document Receipt and Review

    • Scanning and Digitization

    • Indexing and Classification

    • Quality Control (QC)

    • Filing and Organization

    • Document Distribution

    • Archiving Activities

  • Ensure proper document version control and tracking.

Study Team Collaboration

  • Work closely with:

    • Clinical Operations Teams

    • Project Managers

    • Clinical Trial Teams

    • Regulatory Teams

    • Sponsors and Clients

  • Support study teams in fulfilling TMF requirements and resolving document-related issues.

  • Provide guidance regarding TMF processes and documentation standards.

Compliance & Quality Management

  • Ensure all TMF activities comply with:

    • ICH-GCP Guidelines

    • Regulatory Requirements

    • Company SOPs

    • Client Standards

  • Perform quality checks to ensure document accuracy and completeness.

  • Identify and escalate quality concerns or compliance risks.

Reporting & Communication

  • Provide information for:

    • Study Status Reports

    • TMF Metrics

    • Compliance Reports

    • Departmental Reporting Requirements

  • Communicate project updates, quality concerns, and timeline issues to management.

  • Maintain clear and effective communication with internal and external stakeholders.

Audit & Inspection Support

  • Participate in:

    • Internal Audits

    • Sponsor Audits

    • Regulatory Inspections

    • TMF Reviews

  • Support audit preparation and response activities.

  • Ensure TMF documentation is inspection-ready at all times.

Training & Continuous Improvement

  • Participate in required training programs and professional development activities.

  • Stay current with TMF standards, regulations, and best practices.

  • Contribute to process improvement initiatives and departmental projects.

  • Support knowledge sharing within the team.

Additional Responsibilities

  • Provide copies of study documentation to authorized personnel when required.

  • Liaise with clients on project-related TMF activities when directed by management.

  • Support special projects and additional assignments as needed.


Required Qualifications

Education

  • Bachelor’s Degree in:

    • Life Sciences

    • Pharmacy

    • Biotechnology

    • Healthcare

    • Related Scientific Discipline

Life Science degree preferred.


Experience

Required

  • 1–15 years of Trial Master File (TMF) experience.

  • Strong knowledge of clinical trial documentation and TMF processes.

  • Experience supporting clinical research studies within CRO, pharmaceutical, biotechnology, or healthcare environments.