FDA Submissions & Clinical Research Monitor — Hybrid
Virginia Commonwealth University
Virginia Commonwealth University is seeking a FDA Program Administrator/Clinical Research Monitor to support regulatory submissions and monitoring of sponsor-investigator trials. The role focuses on risk-based monitoring, FDA/IRB submissions, and coordination with study teams across research programs. You'll train investigators on Veeva SiteVault, eTMF, and EDC, maintain dashboards, and assist in inspections, with a hybrid work arrangement and a strong emphasis on compliance and collaboration #J-18808-Ljbffr Virginia Commonwealth University
Vacancy posted 2 days ago
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