Meeting Coordinator

Job Summary

A company is looking for a Coordinator II, Meeting Coordinator.

Key Responsibilities

• Support IRB meeting preparation and coordination, including reviewing submissions and sending assignments to reviewers
• Conduct pre-reviews and edits of consent forms to ensure regulatory compliance
• Maintain knowledge of regulatory guidelines and assist with organizational compliance

Required Qualifications

• Minimum of 1 year of IRB or clinical research experience with a bachelor's degree, or 4 years with an associate's degree
• Proficient with MS Word and Outlook
• Basic knowledge of Federal laws and guidelines for Human Subjects Research Protection
• Completion of standard Human Subjects Research Training, such as CITI
• Ability to attend a minimum of four IRB meetings per month