Grant Services & Analysis
We support research teams throughout the proposal process to successfully obtain and maintain extramural funding.
Below are a list of quick links to our most-visited services. We look forward to working with you!
Spotlight On
AI Letter of Support Writer
Research administrators and investigators are encouraged to use the new MM AI Letter of Support Writer, an artificial intelligence (AI) platform, that assists in the creation of letters of support for research proposal submissions.
This course will introduce the basics of conducting human subject research in compliance with federal regulations and institutional practices.
This course offers an overview of informed consent in human subject research. The course will examine IRBMED’s standard consent template and focus on how it reflects federal requirements.
This course is intended for those unfamiliar with eResearch, the university’s electronic research administration site. This course will provide a basic knowledge of working in and using eResearch while examining the process for creating and submitting an initial project application.
Help yourself to a cookie and learn how the Flow Cytometry Core can enhance your research. Core experts will speak about services and instrumentation capabilities.
Event runs January 11, 2025 - December 11, 2025
Have a free cookie and listen to Flow Cytometry Core experts speak about services and instrumentation capabilities.
Event runs January 14, 2025 - April 08, 2025
This course offers an overview of some special situations relating to informed consent. Specifically, waivers and alterations of informed consent, waivers of documentation of informed consent, and obtaining consent from non-English speakers.
This course will identify what constitutes an Adverse Event, ORIO, and Unanticipated Problem and how such events impact risk to subjects. Additionally, the course will review the requirements of reporting such events to the IRB and other entities.
This course is a follow-up to Initial Project Applications and will examine the process for submitting amendments and scheduled continuing reviews to IRBMED using eResearch once a project’s initial application has been approved.
This course will review when studies are required to have a DSMP or DSMB and how to develop an appropriate DSMP. A DSMB is an independent group that advises the study team regarding subject safety, study conduct, and efficacy. The DSMB will also make recommendations concerning the continuation, modification, or termination of the trial. A DSMP outlines how subject safety and data integrity will be maintained to ensure the validity of collected data.
Office of Research
The AVITI24 Grant Program is an opportunity for you to push your research further and faster.
Office of Research
Medical School releases 2024 Research Annual Report
Office of Research
Cassie Wong named the Senior Director for Research in the Medical School Office of Research, effective December 1, 2024.