Senior IRB Administrator
On-siteLittle Rock, Arkansas, United States
Job Summary
Prereview and review research submissions, including new protocols, amendments, and continuing reviews, ensuring compliance with federal, state, and institutional regulations. Process determinations for each submission and communicate with Principal Investigators to resolve information gaps. Facilitate ethical human subject research by training others, supporting IRB meetings, and maintaining reviewer records and rosters. Provide regulatory guidance to faculty, staff, and students while collaborating with HRPP components to revise policies and develop protocol templates. Maintain internal quality assurance activities and pursue continuing education to improve knowledge bases. Serve as an ambassador to the research community and act as a liaison between the research team and the IRB chair.
Required Qualifications
- Bachelor's Degree
- 6 years of experience
- Minimum of 3 years work experience in human research, animal research, research administration or other regulatory based field
- Expertise working with Microsoft Office including Word, Excel, PowerPoint and Outlook
- Excellent analytical and communication skills, both verbal and written
- Organization skills
- Ability to lead, teach and motivate others
- Proof of legal authority to work in the United States
Desired Qualifications
- Experience as a research project manager or research coordinator
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