Welcome Back

Google icon Sign in with Google
OR
I agree to abide by Pharmadaily Terms of Service and its Privacy Policy

Create Account

Google icon Sign up with Google
OR
By signing up, you agree to our Terms of Service and Privacy Policy
Instagram
youtube
Facebook

Tmf Specialist I

Icon
ICON
1-3 years
preferred by company
10 Jan. 30, 2026
Job Description
Job Type: Full Time Hybrid 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 I | ICON plc | Chennai, India

Location: Chennai, India
Work Model: Office with Flex (Hybrid)
Employment Type: Full-Time
Experience Required: 1–3 years in clinical research, TMF, or document management
Job Requisition ID: JR142500


About ICON plc

ICON plc is a world-leading healthcare intelligence and clinical research organization committed to advancing clinical development and improving patient outcomes globally. With a focus on innovation, inclusivity, and excellence, ICON empowers teams to deliver high-quality services for clients and stakeholders worldwide.


Role Overview

ICON is seeking a TMF Specialist I to join our dynamic team in Chennai. In this role, you will gain hands-on experience with Trial Master File (TMF) documentation and document management processes. You will contribute to both client service contracts and internal business requirements while ensuring full compliance with regulatory and organizational standards.

This position is ideal for candidates with early-career experience in clinical research, document management, or TMF operations, seeking to build expertise in a global clinical research environment.


Key Responsibilities

  • Support and maintain Trial Master File (TMF) documentation in accordance with ICON SOPs and client requirements

  • Assist in organizing, reviewing, and filing TMF documents to ensure completeness and compliance

  • Contribute to client services contracts and internal ICON documentation needs

  • Collaborate with cross-functional teams to ensure timely and accurate document management

  • Develop familiarity with TMF processes, study-specific requirements, and regulatory expectations

  • Support audits and inspections by ensuring TMF readiness and adherence to quality standards


Required Qualifications & Experience

  • Bachelor’s degree in Life Sciences, Pharmacy, Medicine, or related field

  • 1–3 years of experience in clinical research, document management, or TMF operations preferred

  • Strong organizational skills with attention to detail

  • Ability to work effectively within a team-oriented environment

  • Excellent written and verbal communication skills in English

  • Familiarity with regulatory compliance and clinical study documentation is an advantage


Why Join ICON?

ICON offers a dynamic, inclusive, and growth-oriented work environment where your contributions make a direct impact on global clinical development.

Benefits include:

  • Competitive salary and annual performance-based incentives

  • Comprehensive health insurance options for employees and families

  • Retirement planning and life assurance benefits

  • Flexible work arrangements and work-life balance initiatives

  • Access to the Global Employee Assistance Programme (TELUS Health) for 24/7 support

  • Country-specific optional benefits: childcare vouchers, gym memberships, bike purchase schemes, subsidized travel passes, and health assessments

ICON is an equal opportunity employer committed to creating an inclusive and accessible workplace. Reasonable accommodations are provided for applicants with disabilities throughout the recruitment process.


Apply Now to join ICON as a TMF Specialist I in Chennai and build a career in clinical research while contributing to high-quality global clinical operations.