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Grants
Effective sponsored project management is a collaboration among Principal Investigator(s); Departmental Administrators and other research staff; Sponsored Programs Administration (SPAdmin); and Sponsored Programs Accounting (SPAccting). SPAdmin Role Provid...
Industry Contracts
SPAdmin negotiates a wide range of research-related agreements on behalf of UNMC faculty-investigators and is a resource to help determine who can best support your contracting needs. SPAdmin Negotiation Process When a contract is initiated, either the PI or...
Clinical Trial Contracts
Getting Started Who can help me with industry-sponsored clinical trials? Your department administrator and the UNeHealth Contracts Office Associate should be notified as soon as you identify a study in which you plan to participate. Web: unmc.edu/spa/clinic...
Clinical Trials
Information relevant to clinical trials can be found on the pages within this section. While SPAdmin is involved in parts of these projects, the majority of the effort is handled by UNeHealth and the CRC's clinical research billing team. UNeHealth (Industry-S...
Industry Sponsored Research
Who can help me with industry-sponsored research? Your department administrator and the SPAdmin Contracts Associate should be notified as soon as you identify a study in which you plan to participate. Web: unmc.edu/spa/contracts/non-clinical Phone: 402-559-...
About Us
Sponsored Programs Administration (SPAdmin) offers services to faculty and grant administrators to support their pursuit and management of external funding. SPAdmin is the official authorized signature authority of UNMC for sponsored program grants and contra...
1.1 Human Research Protection Program (HRPP)
Last Revised: 2/18/2026 1.0 Purpose The purpose of this policy is to provide a basic description of the Organization’s Human Research Protection Program (HRPP) through: 1) the Organization’s stated mission, 2) application of ethical principles to guide all hum...
Policies
Administration of sponsored programs requires compliance with applicable UNMC and sponsor policies. The order of precedence is as follows: Award terms & conditions Program guidelines Sponsor/Agency terms & conditions Uniform Guidance Plus any applica...
1.2 Authority Granted to the IRB and/or the Office of Regulatory Affairs (ORA) by the Organization
Last Revised: 12/17/2025 1.0 Purpose The purpose of this policy is to describe the authority granted by the Organization for the IRBs and the Office of Regulatory Affairs (ORA) operating within the HRPP. 2.0 Policy It is the policy of the Organization that: ...
1.3 UNMC IRB Serving as the Single IRB for Multisite Research
Last Revised: 4/21/2025 For an abbreviated version intended for investigators, coordinators, and study teams - please visit here: sIRB 1.0 Purpose The purpose of this policy is to describe the Organization’s requirements for the UNMC IRB to serve as the Single...
1.4 UNMC Ceding Review to an External Central IRB
Last Revised: 5/15/2025 For an abbreviated version intended for investigators, coordinators, and study teams - please visit here: cIRB 1.0 Purpose The purpose of this policy is to describe the Organization’s requirements for the UNMC IRB to cede review to an e...
1.5 Requirements for Research Conducted with International Sites
Last Revised: 6/10/2026 For an abbreviated version intended for investigators, coordinators, and study teams - please visit here: International Research 1.0 Purpose The purpose of this policy is to describe the Organization’s requirements for research conducte...
1.6 IRB Composition, Leadership, Qualifications, and Responsibilities
Last Revised: 2/15/2025 1.0 Purpose The purpose of this policy and procedure is to describe the Organization’s requirements for IRB composition, leadership, member qualifications, and responsibilities. 2.0 Policy It the policy of the Organization that the mem...
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 requirements for the identification and management of IRB member, consultant, staff and guest potential conflicts of interest. For the purpose of this policy, sta...
1.8 Investigational Activities Requiring IRB Review and Approval
Last Revised: 5/9/2023 For an abbreviated version intended for investigators, coordinators, and study teams - please visit here: What Requires IRB Review and Approval 1.0 Purpose The purpose of this policy is to describe the investigational activities that req...
1.9 Resources Necessary to Protect Subjects
Last Revised: 1/16/2025 1.0 Purpose The purpose of this policy is to describe the Organization’s requirements for resources that are necessary for human subject protection, care of research participants, and safety during the conduct of research. 2.0 Policy I...
General Information
1.10 Scientific and Other Committee Review of Research
Last Revised: 4/8/2025 1.0 Purpose The purpose of this policy is to describe the Organization’s requirements for scientific and scholarly merit review, and for review by other component committees of the HRPP, of all non-exempt human subject research conducted...