Category: Event

This workshop outlines the process of obtaining valid informed consent and will give you the opportunity to demonstrate necessary language and communication skills when interacting with potential study participants and their families. This session is not about writing...
A workshop that will build your capacity to work in a high-performing, cross-disciplinary team This 2-day workshop will take place 9:30 a.m. – 5 p.m. on May 12 and 13, 2025. Through gameful simulations and practice, this 2-day, in-person workshop will build your...
Are you interested in enhancing and refining your mentoring abilities? Do you need to fulfill a mentor training requirement? The MICHR Mentoring Academy curriculum helps senior postdocs, senior staff, and faculty in clinical and translational research develop and hone...
Join us for an exciting opportunity to learn all about the FAST PACE Toolkit! This virtual event will dive into the world of FAST PACE and cover key guidelines for establishing and maintaining a community-academic research partnership and guidelines and...
How to Tailor Communications to Specific People or Groups As researchers, you have a lot of different audiences that may benefit from knowing about your work. You may want to build connections with funders, patients, community members, researchers in other fields, or...
Join us for an exciting event where you can learn all about the FAST PACE Toolkit. This in-person training will take place at the Hasselbring Senior Center located in Flint on Monday, January 27th from 2:30-4:30 p.m. Get ready to dive into the world of community...
Collaborative research, which includes Community Based Participatory Research (CBPR) and Community Engaged Research (CEnR), is a process to address community priorities and issues. After participating in this session, attendees will be able to discuss: the rationale...
This session will introduce participants to best practices for creating, interpreting, and using a manual of procedures (MOP) and other procedures documentation to ensure standardized practices across personnel and sites of a clinical trial. Topics will include an...