Careers in Quality

This job assumes responsibility for performing thorough review of clinical research studies submitted to the IRB Office for the purposes of assuring compliance to regulatory requirements, clarity of informed consents and completeness of IRB application forms. Works in coordination with Investigators and Research Coordinators to assure completeness and quality of submissions to the IRB Panels for review; and assumes responsibility for database management, formal letter generation, and individual instruction for investigators and coordinators on the IRB process and use of IRB database. Job Duties Reviews research study submissions prior to IRB review for completeness and compliance to regulatory requirements. Reviews and edits research