Grant Services & Analysis

We support research teams throughout the proposal process to successfully obtain and maintain extramural funding.

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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.

How Grant Services & Analysis Supports Research
Research Development

Our Research Development professionals work with faculty to increase extramural funding. We connect faculty with opportunities; work with faculty on grant writing/editing; coordinate large-scale proposals; support faculty career development through programs like R01 Boot Camp; manage internal funding programs; provide bridging support; and assist with limited submissions.

Pre-Award

“Pre-Award” constitutes anything that facilitates a proposal’s creation and submission, prior to the award being received. We offer resources for proposal preparation, using eResearch Proposal Management (eRPM), proposal routing, and proposal submission.

Post-Award

“Post-Award” comprises everything that happens to administer a research project, following the official award being received. We also maintain the Post-Award Procedures Manual, which represents the consolidation of the Medical School post-award procedures and best practices.

Research Data Analytics

Our office provides data for sections of the M-DASH and M-STAT systems. We collect data from the proposals submitted, as well as directly from the National Institutes of Health. We are also able to provide data based on award submissions and receipts.

Resources & Education

Our office also writes and maintains policies related to aspects of sponsored research in the Medical School, creates and holds training sessions on various research administration topics, and works on special projects that arise and need our expertise.

Frequently Asked Questions

Review answers to the most common questions regarding grant routing and review policy, budget/justification issues, NIH proposals and awards, eRPM, PAF, PHS, FCOI, access to data systems, and post-award.

Upcoming Research Events All Office of Research Events
Federal and Institutional Requirements for Human Subject Research
This course will introduce the basics of conducting human subject research in compliance with federal regulations and institutional practices.
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Elements of Informed Consent
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.
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Introduction to eResearch
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.
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Flow and Cookies at NCRC
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
Flow and Cookies on Med Campus
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
Waivers, Alterations, and Alternative Forms of Informed Consent
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.
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Reporting AEs, ORIOs, and Unanticipated Problems
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.
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Amendments and Continuing Reviews
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.
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Data and Safety Monitoring Boards and Data Safety Monitoring Plans
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.
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Featured Research News All Office of Research News " "
Office of Research
University of Michigan AVITI24 Grant Program
The AVITI24 Grant Program is an opportunity for you to push your research further and faster.
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Office of Research
2024 Research Annual Report Released
Medical School releases 2024 Research Annual Report
Cassie Wong
Office of Research
Cassie Wong Appointed Senior Director for Research in the Medical School Office of Research
Cassie Wong named the Senior Director for Research in the Medical School Office of Research, effective December 1, 2024.