Regulatory Research Coordinator

What you’d do

Facilitates the opening of cancer clinical research protocols, preparing IRB submissions, informed consents, and regulatory packages for study sponsors. Coordinates study initiations, monitoring visits, and regulatory files across MSMC and MS-Aventura. Full time. Found on the employer's careers page on Oct 6, 2026. Apply through the link.

You’ll need

• Bachelor's degree preferred
• Regulatory experience preferred
• IRB submission experience
• Clinical research protocol coordination