TMF/eTMF Program Lead - Veeva Vault & Inspection Readiness
Listed on 2026-11-01
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Quality Assurance - QA/QC
QA Specialist - Analyst/Manager, Quality Control - QC Analysts/Managers, Regulatory Compliance Specialist -
Pharmaceutical
Regulatory Compliance Specialist
Bio Cryst Pharmaceuticals, Inc. seeks a TMF Manager to lead and oversee TMF/eTMF strategies, ensuring high-quality, inspection-ready documentation across Phase I–IV studies.
You will drive standardization of TMF/indexing, and collaborate with CRA, CROs, and IT on system configurations and training. Ideal candidates have 5+ years TMF/eTMF experience, familiarity with DIA TMF Reference Model and Veeva Vault Clinical, and strong regulatory knowledge.
Step into the TMF/eTMF Program Lead
- Veeva Vault & Inspection Readiness role at Bio Cryst Pharmaceuticals, Inc. in NC, United States and grow with us.
The following position is for a TMF/eTMF Program Lead
- Veeva Vault & Inspection Readiness with Bio Cryst Pharmaceuticals, Inc.
Our team is growing, and we are hiring a TMF/eTMF Program Lead
- Veeva Vault & Inspection Readiness in NC, United States.
This position is for the TMF/eTMF Program Lead
- Veeva Vault & Inspection Readiness role at Bio Cryst Pharmaceuticals, Inc.
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