TMF Specialist
TMF Specialist
ICON
Job description
Looking to build a career in clinical trial document management? Explore this TMF Specialist role at ICON in Chennai, open across all experience levels.
Company Description
ICON is a company that works in healthcare intelligence and clinical research. The team takes pride in building a place where real innovation can grow and excellence is encouraged. They all work together toward one goal: shaping the future of development. ICON grows worldwide working to bring medicines and treatments to patients faster through close collaboration and scientific expertise.
Job Summary
This hybrid role is based in Chennai, inside ICONs Regulatory Document Management team. As a TMF Specialist you will manage Trial Master File documents from start to finish of a trial. Your tasks will involve receiving, reviewing, indexing and archiving documents following ICON SOPs and client requirements. This position is open to all experience levels. Is suitable for newcomers learning TMF or experienced professionals handling complex study documentation.
Key Responsibilities
Become familiar with Trial Master File documentation and management processes.
Support client services contracts and internal ICON business needs related to TMF.
Ensure compliance with client requirements and ICON procedures at every step.
Handle document receipt, review, scanning, indexing and quality control.
File, copy, forward or archive documents as required by the study.
Maintain study files in line with client requirements and ICON SOPs.
Liaise with study teams and other TMF staff to fulfill responsibilities.
Departmental projects within specified timelines and regulations.
Prepare client and departmental status reports, as requested by management.
Inform managers of training needs, project updates and quality issues.
Take part in audits and document archiving activities as needed.
Provide copies of study documents to ICON or client personnel when requested.
Take part in training sessions to build TMF related skills.
Liaise with clients on project issues as directed by the manager.
Handle projects or additional duties as assigned.
Educational Qualification
A degree in life sciences or a related field, alongside relevant clinical research experience.
Skills Required
1 to 15 years of TMF experience with knowledge of clinical study documents.
Ability to work well with project teams, staff, clients and management.
Good verbal and written communication skills.
Strong interpersonal skills to coordinate across multidisciplinary teams.
Strong attention to detail while managing critical documents.
Good organizational and time management skills.
Familiarity with clinical trial regulations and documentation standards.
Comfortable using electronic document management systems and TMF software.
Salary Breakdown by Experience
The average annual salary of TMF Specialist at ICON typically ranges from ₹4.1 Lakhs to ₹4.5 Lakhs per year, depending on experience.
Career Development
This role offers hands on exposure to global clinical trial documentation across a wide range of experience levels. ICON also supports long term growth through a diverse, high performing culture and clear opportunities to advance within document management.
How to Apply
Visit our job portal and search for the TMF Specialist role in ICON.
Click on the job posting to read all the details about the job.
Fill in your details. Upload your updated resume.
Send your application.
Education
Bachelor's Degree
Key Skills
Market insights & trends
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