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Trial Master File (TMF) Specialist III at ICON plc - ApplyBlast

Trial Master File (TMF) Specialist III

ICON plc

28 days ago

Remote

Full Time

Medior

0 applicants

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About this role

The Trial Master File (TMF) Specialist III at ICON Strategic Solutions manages trial master file documentation to ensure quality, accuracy, and regulatory compliance throughout the clinical trial lifecycle. This role involves collaborating with cross-functional teams to collect and review essential documents while providing guidance to stakeholders on TMF-related matters. The position supports sponsor-dedicated contracts within a global clinical research organization.

Responsibilities

Manage Trial Master File documentation in accordance with client requirements and ICON procedures
Ensure completeness, accuracy, and timeliness of TMF documentation throughout clinical trial lifecycle
Conduct quality checks and audits of TMF documents to ensure compliance with regulatory standards

Skills

Qualifications

Bachelor's degree in life sciencesBachelor's degree in documentation managementBachelor's degree in a related discipline

About ICON plc

iconplc.com

Headquarters

South Dublin, Ireland

Company Size

10001+ employees

Founded

1990

View Profile

ICON plc is a global clinical research organisation (CRO) that provides outsourced clinical development and commercialisation services to pharmaceutical, biotechnology and medical device companies. It offers end-to-end drug and device development support — including clinical trial management across phases, data management and biostatistics, regulatory and safety/pharmacovigilance, and commercialisation and market-access services. ICON combines scientific and therapeutic expertise with technology and a scalable global operations network to accelerate development and bring therapies to patients. Clients engage ICON for integrated, experienced CRO support across the full product lifecycle.