BioCryst Pharmaceuticals
The Trial Master File (TMF) Manager is responsible for developing, implementing, and overseeing processes for the consistent creation, maintenance, and archival of BioCryst's TMFs in compliance with SOPs, GCP, and ICH guidelines. This role serves as a subject matter expert for electronic TMF systems, providing hands-on leadership for TMF setup, indexing, tracking, and quality review across Phase I–IV studies. The position partners with study teams, functional areas, and CROs to maintain high-quality TMFs and support regulatory submissions, audits, and inspections.
Headquarters
Durham, North Carolina, United States
Company Size
501-1000 employees
Founded
1986
BioCryst Pharmaceuticals is a global biotech company with over three decades of experience in drug discovery, development, and commercialization, specializing in rare disease therapeutics. Founded in 1986, the company focuses on hereditary angioedema (HAE) and other rare diseases, delivering first-in-class or best-in-class oral small-molecule and injectable protein therapeutics. BioCryst uses a novel, structure-guided approach blending traditional biology and medicinal chemistry with advanced technologies to develop medicines for underserved patient communities worldwide.
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 BioCryst Pharmaceuticals.
BioCryst Pharmaceuticals didn’t post a salary, so this is our estimate from similar listings.
Right around the average for this role