pharmaron
The Trial Master File Specialist ensures Trial Master Files remain compliant, complete, and inspection-ready while supporting the successful execution of clinical trials. This role involves managing sponsor TMFs from study start-up through closeout, developing filing strategies, and serving as the subject matter expert for electronic TMF systems. The specialist conducts quality reviews, generates metrics, and partners with project teams to maintain inspection readiness throughout the study lifecycle.
Headquarters
Rushden, England, United Kingdom
Company Size
10001+ employees
Founded
2004
Pharmaron is a global life science Contract Research Organization (CRO) and CDMO that offers comprehensive research, development, and manufacturing services spanning drug discovery, preclinical, clinical development, and commercialization. The company supports small molecules, biologics, and cell and gene therapy products, providing integrated laboratory, chemistry, manufacturing, and clinical services. Pharmaron serves as a full-spectrum partner to pharmaceutical and biotech companies worldwide in advancing innovative medicines.
Headquarters
San Francisco, CA
Company Size
201-500 employees
Founded
2018
Industry
Technology
Glassdoor Rating
4.2 / 5
Sarah Johnson
Chief Executive Officer
Michael Chen
Chief Technology Officer
Emily Williams
VP of Engineering
David Rodriguez
VP of Product
Jessica Thompson
Chief Financial Officer
Andrew Park
VP of Sales
View leadership team, funding history,
and employee contacts for pharmaron.
43% below the average for this role