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Industry-Sponsored Non-Clinical Research
Industry-sponsored contracts must be reviewed and negotiated before being signed. SPA negotiates ...
Industry Sponsored Clinical Research
Clinical research is defined as research that involves human subjects as participants and/or requ...
Roles & Responsibilities
As soon as you determine interest in a particular project or study, be sure to contact your depar...
Award Close-Out
After the funded project is complete, UNMC must administratively close out the project with the s...
Post Award Guidelines
Reporting Requirements Technical The PI is responsible for preparing the technical report. Eit...
Just In Time
Just in Time refers to the period after application submission and peer review and before selecti...
Pre-Award Guidelines
SPAdmin can assist you with many aspects of developing and submitting a proposal. Once you ident...
3.9 Contraception Requirements
Last Revised: 5/5/2025 1.0 Purpose The purpose of this policy is to describe the contraception re...
sIRB - Submission deadlines
sIRB Submission Deadlines for New Submissions, Previously Tabled Protocols and Requests for Chang...
Does my project require IRB review?
To help you determine if your project constitutes Human Subject Research and requires IRB review,...
3.7 Finder’s Fees and Recruitment Bonuses
Last Revised: 1/26/2018 1.0 Purpose The purpose of this policy and procedure is to describe the O...
3.1 Assessing the Need for Increased Monitoring, Interim Continuing Review, and Verification from Sources Other than the PI
Last Revised: 1/2/2018 1.0 Purpose The purpose of this policy and procedure is to describe the Or...
2.8 Limited IRB Review
Last Revised: 6/5/2023 1.0 Purpose The purpose of this policy is to describe the Organization’s r...
1.20 Community Involvement in Outreach Activities and Community Based Participatory Research (CBPR)
Last Revised: 1/17/2024 1.0 Purpose The purpose of this policy is to describe the Organization’s ...
1.19 IRB Signature Authority
Last Revised: 10/7/2022 1.0 Purpose The purpose of this policy is to describe the Organization’s ...
1.11 HRPP Access to Legal Counsel
Last Revised: 2/11/2025 1.0 Purpose The purpose of this policy is to describe the Organization’s ...
1.7 IRB Member, Consultant, Staff and Guest Conflict of Interest Identification and Management
Last Revised: 9/25/2024 1.0 Purpose The purpose of this policy is to describe the Organization’s ...
Dual-Use Research of Concern
According to the National Institutes of Health, dual use research of concern (DURC) is "life scie...
Developing a Budget
Information pertaining to Human Subject Research, Institutional Review Board, and the Office of R...
Institutional Review Board
Information pertaining to Human Subject Research, Institutional Review Board, and the Office of R...