• Managing Human Research Protection Program (HRPP) policies and procedures
  • Managing pre-review of IRB materials
  • Managing review of IRB materials
  • Managing exempt study review determinations
  • Managing research protocol approval or reliance process
  • Managing regulatory documentation
  • Managing IRB records and databases
  • Facilitating IRB meeting (e.g., ensure quorum, distribute meeting materials)
  • Developing and provide education on IRB regulations and processes
  • Providing consultation on IRB submission
  • Monitoring for changes in federal regulations and guidance
  • Managing review of noncompliance and unanticipated problems
  • Managing IRB meeting minutes