Research Administration Regulatory
Training
Required Training for All Staff Prior to UA IRB submission
- 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)
- 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