Participants will discuss risk in human subjects research and approaches for minimizing or mitigating risk. This event will also examine confidentiality and data security measures to protect research subjects.   Registration

So you know you can't begin collecting your research data before getting IRB approval, but what about using secondary data? Join us for this in-depth discussion about secondary data. This session is most useful for attendees who have completed IRB 101 or have basic knowledge of IRB principles and processes.   Registration

In this session participants will learn tips on developing and submitting protocols to the IRB. A member of IRB staff will walk through key sections of the IRB application and explain what the IRB looks for during the review process.   Registration

In this session participants will learn tips on developing and submitting protocols to the IRB. A member of IRB staff will walk through key sections of the IRB application and explain what the IRB looks for during the review process.   Registration

In this session, participants will learn how to determine whether IRB oversight is required for your project. We'll also examine the various levels of IRB review (Exempt, Expedited, Full Committee).   Registration

This workshop will discuss the extra considerations and practices that occur when working with researchers from outside of ISU. Learn the best practices for submitting IRB protocols with multiple institutions involved and determine how to best ensure research starts without any concerns.   Registration

In this session, participants will learn about the informed consent process, including participant recruitment and the informed consent document. Discussion will center around what's required of you as the researcher, and best practices for designing and administering consent.   Registration

Applying to a Department of Energy (DOE) Office of Science Funding Opportunity Announcements (FOA) or DOE National Laboratory Announcements? Need to learn more about the Promoting Inclusive and Equitable Research (PIER) plan? We'll cover the newly updated requirements for PIER plans in these funding opportunities and discuss how to address them in your proposals. This...

Participants will discuss risk in human subjects research and approaches for minimizing or mitigating risk. We'll also examine confidentiality and data security measures to protect research subjects. Registration

Join us to incorporate useful tools, tips, and tricks into your research teams with Dr. Ellen Fisher and Dr. Hannah Love. Drs Fisher and Love plan to discuss a variety of tools you'll be able to take into practice that are supported through team science research practices.

Planning to do some research involving children? Are you aware of the special requirements and additional steps you'll need to follow? Join us for this discussion into the additional steps and requirements that you will need to be aware of while working with children as human research subjects. There are a few special requirements to...

In this session you will learn tips on developing and submitting protocols to the IRB. A member of IRB staff will walk through key sections of the IRB application and explain what the IRB looks for during the review process.   Registration