A virtual training, PACE Collaborative Research, will help community and academic partners and partnerships strengthen how they conduct collaborative research.

Have you completed basic instruction in clinical research but are looking for more? The Instruction in Monitoring, Procedures Documentation, and ClinicalTrials.gov (IMPACT) workshop series is designed for study team members who are ready for an intermediate level of training for clinical trials skills. Participants will learn critical clinical research skills through a group learning environment and hands-on skills practice. Sessions will be virtual and information will be emailed to registrants before the event. Registrations are required.

The Michigan Institute for Clinical & Health Research (MICHR) is hosting the inaugural kickoff for its University of Michigan (U-M) Implementation Science Network (ISN). This free event is intended for faculty, staff, and learners who are enthusiastic about D&I science (including knowledge translation, improvement science, engagement science etc.). Affiliation with U-M not required. Networking session with light refreshments to follow closing remarks.

This workshop will teach you best practices in preparing a new study before you submit an IRB application. Learn expert tips from an experienced coordinator to save time, effort and money later in your study. This session will include hands-on training including breakout rooms, so please be prepared to participate and interact. This session will not be recorded.

This session 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 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 workshop will teach you best practices in preparing a new study before you submit an IRB application. Learn expert tips from an experienced coordinator to save time, effort and money later in your study. This session will include hands-on training including breakout rooms, so please be prepared to participate and interact. This session will not be recorded.

This workshop for faculty will address the challenge of communicating about your research with different audiences.. 

This session 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.

ClinicalTrials.gov requirements and publisher expectations are changing the way studies are designed and implemented. Policies encouraging transparency and data sharing are affecting trial registration, updates, results reporting, and uploads of the protocol and informed consent. Group exercises and discussion with regulatory and data sharing specialists will help participants learn how to meet these requirements while strengthening scientific practices.

This session 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 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 structured, introductory three-part workshop is designed to assist early career faculty and fellows who are preparing competitive career development grant applications (NIH K, VA CDA, and MICHR K) for 2022 submission. As a participant, you will exchange drafts of sections of your proposal and receive peer critique and feedback from senior faculty experienced in NIH study section thinking.

ClinicalTrials.gov requirements and publisher expectations are changing the way studies are designed and implemented. Policies encouraging transparency and data sharing are affecting trial registration, updates, results reporting, and uploads of the protocol and informed consent. Group exercises and discussion with regulatory and data sharing specialists will help participants learn how to meet these requirements while strengthening scientific practices.

The 2021 Mentoring Forum and Mentor Awards Ceremony will celebrate mentorship and celebrate the 2020 and 2021 MICHR Distinguished Clinical & Translational Research Mentor Award recipients. All faculty, staff and students are welcome and encouraged to attend.

Have you completed basic instruction in clinical research but are looking for more? The Instruction in Monitoring, Procedures Documentation and ClinicalTrials.gov (IMPACT) workshop series is designed for study team members who are ready for an intermediate level of training for clinical trials skills. Participants will learn critical clinical research skills through a group learning environment and hands-on skills practice.

Join MICHR for an online interactive workshop presenting the basics of budgeting for research grants. Learn how to calculate indirect costs, determine calendar months for effort, complete other budget components, and write a budget justification. We will also talk about how to monitor expenses after you are awarded and the closeout (FFR) process. This budgeting workshop is modeled using a NIH budget format.

This session 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 seminar is designed for study team members who desire a reintroduction to basic statistical concepts for clinically-focused research. Presented in plain English with many illustrations, this session will cover foundational statistical concepts, including p-value, effect size, confidence intervals, sample size and power, and some common statistical tests.

Conducting and Obtaining Valid Informed Consent 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.

In Winter 2021, MICHR will offer the popular Responsible Conduct of Research (RCR) for K Awardees, a seminar that is designed to meet the requirements of the NIH K-23, or any federal or non-federal career development grant.