Past Events

The goal of this session is to help researchers improve the impact of their research through publication. Section 1: Impactful titles (15 min) This section discusses how to write a title that gets the reader’s attention in online databases and increases the chances that they will click on it and read the abstract of the […]

In this workshop, you will learn best practices in preparing for a new study before you submit an IRB application or for beginning a new phase of the research. You’ll get expert tips from an experienced coordinator that will help you save time, effort and money later in your study. This engaging and interactive session […]

The Michigan Institute for Clinical & Health Research (MICHR) is hosting a symposium on using Artificial Intelligence (AI) and Machine Learning (ML) as an implementation strategy at the annual meeting for the Implementation Science Network. The purpose of this symposium is to gather faculty, staff, learners, and community partners to share experiences and discuss strategies […]

Dr. Tom Valley, Associate Professor of Internal Medicine at the University of Michigan Medical School, will present “Using Clinical Data to Examine Racial and Ethnic Disparities in Critical Illness” as part of the Office of Research Voices in Clinical and Translational Research Speaker Series. The Office of Research’s Voices in Clinical and Translational Research Speaker […]

Part 2: Individual Participant Data Sharing Plans: What, Why, and How to Write One ClinicalTrials.gov requirements and publisher expectations are changing the way studies are designed and publicized. Policies encouraging transparency and data sharing affect trial registration, updates, results reporting, and informed consent. Even if you have assistance with your ClinicalTrials.gov registration, you will save […]

Join the John Hopkins University (JHU) Trial Innovation Center for a virtual symposium highlighting contemporary methods for the efficient design and analysis of clinical trials. New tools and software will be discussed, and attendees will be provided with real-world examples using these innovative methods to aid in producing effective trials. MICHR-affiliated faculty member Kelley M. […]

This is an opportunity to practice thinking like an NIH grant reviewer on a mock “study section.” As one of six grant reviewers, you will discuss actual twelve-page K and R grants (already submitted in some version to the NIH). You will practice for the real K or R grant review process with your peers […]

Obtaining informed consent for research is a multifaceted obligation for researchers, and it is the foundation for the ethical practice of human subjects research. The standard one-sized fits all approach puts the researcher obligations front and center while relegating the prospective participant to a signature on a page. Join us and your peers in a […]

Part 1: Outcome Measures – Why Plain Language Matters in the Age of Transparency ClinicalTrials.gov requirements and publisher expectations are changing the way studies are designed and publicized. Policies encouraging transparency and data sharing affect trial registration, updates, results reporting, and informed consent. Even if you have assistance with your ClinicalTrials.gov registration, you will save […]

All are invited to celebrate our awardees and the spirit of mentorship at the September 27, 2024, Mentoring Forum featuring Elizabeth Harry, MD, Chief Wellness Officer, Medical School, University of Michigan. Dr. Harry will present on the importance of well-being. Following Dr. Harry’s talk, the seven mentors who contribute enormously to the research environment at […]