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IRB Process Training
New IRB Training Opportunities
The Office for Responsible Research (ORR) is launching a training program this spring for new, as well as experienced, investigators including graduate students, faculty, and staff who conduct research involving human subjects. Two types of training are offered.
IRB 101: Navigating the IRB Submission Process
IRB 101: Navigating the IRB Submission Process is offered on a recurring basis, on the second Thursday of each month. As part of this presentation, participants learn tips on developing and submitting protocols to the IRB. A member of the IRB staff will walk through key sections of the non-exempt IRB application and explain what the IRB looks for during the review process.
Upcoming Class Dates:
May 11, 2017 from 11:00 am to 12:30 pm in the Ensminger Room, Kildee Hall
June 6, 2017 from 11:00 am to 12:30 pm in 2015 Morrill
August 9, 2017 from 11:00 am to 12:30 pm in 2015 Morrill
Register at Learn@ISU, but if you don't get a chance to register, you are still welcome to attend!
IRB Basics Series
Additionally, we are offering a 4-part series (one session held each quarter) covering IRB Basics. This series addresses different components of human subjects research in a more in-depth manner. Topics are as follows:
1. IRB Basics: Does this project need IRB Oversight?
In this session, participants learn the process to determine whether IRB oversight is required. Additionally, information about the various
levels of IRB review (Exempt, Expedited, Full Committee) is shared.
2. IRB Basics: Protecting Human Subjects
This session includes discussion of risk in
human subjects research and approaches for minimizing risk. The session also
participant confidentiality, as well as data security measures.
Upcoming Class Dates:
May 17, 2017 at 11:30 am in 1030 Morrill Hall
3. IRB Basics: The Informed Consent Process
Learn about the informed consent process, which includes participant recruitment as well as the informed consent document.Discussion will
include regulatory requirements and best practices for designing and administering informed consent.
4. IRB Basics: Best Practices for a Successful IRB Submission
In this session, participants will learn about best practices and receive tips for ensuring a smooth IRB review process.
Those who are interested can register through Learn@ISU. However, if you don't get a chance to register, you are still welcome to attend. If you have any questions about the training, please contact Jennifer Ensley Gorshe, email@example.com 294-7792.