U of A may submit one proposal.
M. Rigdon (Center for Philosophy of Freedom)
Required U or A pre-proposal elements
The UA pre-proposal contains the following required sections and will be entered into text boxes on the application. Only text is accepted (no images, figures, tables, etc.):
An Eligible Entity may submit only one application for Competitive Grant Program funding (regardless of whether the appli
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Husain Al Yusuf (ECE/CompSci/SIE)
Yu-Zheng Lin (ECE/SIE)
Sujan Ghimire (SFWE/SIE)
Trevor Stanfil (OpSci/Physics)
Nominations are being accepted for the IBM Ph.D. Fellowship Awards Program
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Patriricia Thompson-Carino (Cancer Center)
Typically, U of A researchers must receive U of A IRB approval to conduct research with human subjects, regardless of where the research takes place. When collaborative projects are expected to involve researchers from multiple institutions, contact the HSPP to determine next steps. While in some cases each investigator should work with their own institution’s IRB, in other cases, it might be advisable (or required by a funder) to arrange an IRB reliance/institutional agreement (IAA) to designate one IRB to review and approve the research as a whole.
The HSPP does not accept modifications to determinations of human research as these projects are not overseen by an IRB. Investigators may proceed as long as the intent behind the project remains unchanged. If changes are made affecting whether the activities are human research, a new determination request must be submitted for review in eIRB.
Human subjects training is required for all investigators, faculty, staff, and students conducting research with human subjects at the University of Arizona. There are two CITI training options for investigators to choose from, depending on the type of research:
The IRB must review and approve all changes to previously approved Full Committee or Expedite research prior to implementing the changes. For additional information, see our guidance on Modifying Approved Research.
Projects that meet the definition of regulated human research under the Common Rule may fit within one or more categories of “Exempt” research. This does not mean that these studies do not need IRB review. For a research study to be deemed "Exempt", investigators need to submit an application to the IRB. Please note that an "Exempt" determination must be made by the IRB.
Approval timelines are contingent upon the complexity of a study, the investigator's responsiveness, and whether applicable approvals have been obtained. Average approval timelines are broken down by level of review: