TMF/eTMF Program Lead — Audit- Trial Files
Listed on 2026-09-30
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Healthcare
Healthcare Compliance -
Pharmaceutical
Healthcare Compliance
Bio Cryst Pharmaceuticals is seeking a Trial Master File (TMF) Manager to develop, implement, and oversee TMF processes, systems, training, and archival of TMFs for Phase I–IV studies. You will serve as the TMF SME for eTMF and CTMS, ensuring inspection readiness and regulatory compliance across global trials.
The role partners with study teams, CROs, and IT to maintain complete, high-quality TMFs, produce dashboards, and support regulatory submissions and audits.
The following role is for a TMF/eTMF Program Lead — Audit-Ready Trial Files with Bio Cryst Pharmaceuticals.
Consider building your career as a TMF/eTMF Program Lead — Audit-Ready Trial Files at Bio Cryst Pharmaceuticals.
The TMF/eTMF Program Lead — Audit-Ready Trial Files position in the Finance, Bio & Pharmacology & Health field is open for applications.
We have an opening for a TMF/eTMF Program Lead — Audit-Ready Trial Files in NC, United States within Finance, Bio & Pharmacology & Health.
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