Meeting Coordination Specialist

Job Summary

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

Key Responsibilities

• Support IRB meeting preparation and coordination by reviewing submissions and assigning them for review
• Assist in the preparation of informed consent forms and ensure regulatory compliance
• Maintain knowledge of relevant regulations and contribute to process improvements

Required Qualifications

• 1+ year of IRB or clinical research experience with a bachelor's degree, or 4+ years with an associate's degree
• Proficient in MS Word and Outlook
• Basic knowledge of Federal laws and guidelines related to Human Subjects Research Protection
• Ability to work remotely and effectively with remote workers
• Completion of standard Human Subjects Research Training, such as CITI