Research Regulatory Coordinator

Role Overview

The Research Regulatory Coordinator is responsible for ensuring compliance with institutional, state and federal regulations and guidance in the conduct of human subjects research. The Coordinator maintains relationships with external Institutional Review Board (IRB) and other regulatory bodies.

What You Will Do

Serve as the main point of contact with the External IRB, facilitate research readiness review process, document IRB related submissions, and track IRB-related invoices.

Why It Might Be a Fit

Strong interpersonal and professional communication skills, detail oriented, and able to work independently are required. The Coordinator will serve as a subject matter expert to investigators and collaborators for access and use of Rogers patient data for research purposes.

Requirements

• Bachelor's degree
• Three (3) years of work experience in a clinical research setting
• Strong interpersonal skills
• Excellent verbal and written command of the English language
• Demonstrated knowledge of Microsoft Office, Excel, Adobe Acrobat, internet, and other computer software

Benefits

• Health, dental, and vision insurance coverage for you and your family
• 401(k) retirement plan
• Employee share program
• Life/disability insurance
• Flex spending accounts
• Tuition reimbursement
• Health and wellness program
• Employee assistance program (EAP)