IRB Meeting Coordinator

Job Summary

Supporting the IRB Services team, the full-time remote IRB Meeting Coordinator will manage meeting preparation, review submissions for compliance, and assist with informed consent form preparation.

Key responsibilities

• Coordinate IRB meeting assignments and ensure submissions are ready for review
• Prepare and edit informed consent forms in compliance with regulatory standards
• Attend IRB meetings to enhance knowledge of processes and contribute to quality control checks

Required qualifications

• 1+ year of IRB or clinical research experience with a bachelor's degree, or 4+ years with an associate's degree
• Basic knowledge of Federal laws and guidelines related to Human Subjects Research Protection
• Proficiency in MS Word and Outlook; familiarity with Excel and remote meeting applications
• Completion of standard Human Subjects Research Training, such as CITI
• High level of professionalism and ability to manage conflicting demands and priorities