Trial Master File Specialist

Company

Pharmaron

Where

Baltimore, MD

Level

Mid

First seen

September 15, 2026

Listed via

isolved

What the posting says

What You'll Do In this role, you will play a critical part in ensuring TMFs remain compliant, complete, and inspection-ready while supporting the successful execution of clinical trials. Key Responsibilities Own and manage sponsor Trial Master Files (TMFs) from study start-up through closeout. Develop and maintain TMF Plans and filing strategies. Serve as the subject matter expert for electronic TMF (eTMF) systems and processes. Ensure TMFs are maintained in accordance with ICH-GCP, regulatory requirements, and the CDISC TMF Reference Model. Conduct ongoing TMF quality reviews to ensure…

Read more and apply on Pharmaron's site

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