IRB Coordinator

What you’d do

Coordinates administrative review of human research submissions, handling intake, routing, tracking, and follow-up, and serves as the main liaison among investigators, reviewers, and external partners. Full time. Found on the employer's careers page on Oct 7, 2026. Apply through the link.

You’ll need

• High School Diploma/GED
• 2 years IRB or clinical research experience
• Strong attention to detail and organization
• Ability to manage multiple deadlines
• Clear written and verbal communication