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Research Administration Regulatory

Training

Required Training for All Staff Prior to UA IRB submission

  1. CITI Human Subjects (Biomedical Research Investigator) Training
  2. HIPPA Training
  3. COI Training
  4. Research Security Training
  5. Information Security Awareness

  • CITI GCP Training – required for all staff on clinical trials CITI tipsheet
  • Optional Additional GCP Training
  • CITI Clinical Research Coordinator Foundations – required for all staff of a clinical trial who will be directly involved with research participants if the PI is not an MD/DO; recommended for all staff on any study who will be directly involved with research participants (CITI Tipsheet)
  • Tribal Consultation Policy Training – required for all study team members engaged in research involving Native or Indigenous populations, including projects that intentionally target Native populations for participation, involve genetic testing that may reveal tribal affiliation, or could lead to conclusions about a Native Nation
  • UA Box Health – required for all staff using UA Box Health to store or access study data
  • IATA Training - required for coordinators if biological samples and/or dry ice will be shipped
  • OnCore Training – required for at least one staff member to be able to enter subject data
  • eReg Training – required for staff who will sign or view documents in the UAHS electronic regulatory binder
  • Biosafety Training – required for staff who will be performing relevant study activities
  • REDCap Training – required for all staff using REDCap for eConsenting or data collection
  • Zoom for Health training – required for staff who will be setting up HIPAA-compliant Zoom meetings