Manager Sponsor Regulatory Affairs & Institutional Trial Compliance

What you’d do

Leads the Office of Regulatory Affairs and Research Oversight, overseeing sponsor regulatory compliance for institutionally sponsored clinical trials across the health system. Covers trial startup, safety oversight, multi-site expansion, reporting, quality systems, and inspection readiness. Full time. Found on the employer's careers page on Oct 7, 2026. Apply through the link.

You’ll need

• 6 years progressive clinical research experience
• 3 years leadership in regulatory affairs or sponsor operations
• 3 years experience with IND, IDE, or FDA submissions
• Knowledge of FDA regulations and ICH Good Clinical Practice