Calendar Review & Analysis Office
Our analysts and support specialists are here to assist investigators and study teams conducting clinical research.
The Clinical Research Calendar Review & Analysis Office (CRAO) assists principal investigators and study teams conducting clinical research by providing analysts and support specialists who facilitate the building and completion of the billing grid (calendar) that interfaces with MiChart, review required core documents for alignment with Medicare and University policies and provide clinical research billing analysts who will audit and work to have clinical research billing errors corrected.
This course will examine the additional regulatory requirements for conducting research involving pregnant women, fetuses, neonates, children, and prisoners, including the requirements for these populations in a research project and obtaining informed consent.
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.
Join us at our Holiday Open House event, where innovation meets expertise! This is an opportunity for researchers to explore our cutting-edge facilities and discover the exciting advancements in Single Cell, Spatial, and Next Generation Sequencing (NGS) technologies.
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.
The Research Operations, Management & Strategy (ROMS) Fellowship sponsored by the UMMS Office of Research is now recruiting for the 2025-2027 cohort and is hosting an upcoming information session about the program.
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.
Office of Research
The Medical School Office of Research is seeking applications for a faculty leader to serve as an Assistant Dean for Clinical Research.
Office of Research
In observance of university holidays (Thanksgiving and Winter Break), several cores will have a change in operations.
Office of Research
The Aikens Innovation Academy is a project-based course offering mentorship and funding for academics with cardiovascular innovations.