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IRB Training Schedule
Ñý¼§Ö±²¥'s Institutional Review Board staff will offer six trainings
during the Fall 2025 semester. RSVP here, and see below for more information about
each training!
Preparing a Successful IRB Submission
Wednesday, September 10, 2025
1:00 p.m.
This training session is designed to guide researchers through the process of submitting
an initial IRB application in Cayuse. Participants will learn how to accurately complete
and submit their study protocol for IRB review. By the end of the session, attendees
will be equipped with the knowledge and skills needed to successfully navigate the
Cayuse platform and submit a complete, thorough IRB application. This training is
ideal for new researchers or anyone unfamiliar with Cayuse.
Training will be recorded and available for viewing |
Informed Consent: Best Practices
Tuesday, September 23, 2025
2:00 p.m.
This training session focuses on the fundamental principles and best practices for
obtaining informed consent in human subjects research. Researchers will learn how
to develop clear, comprehensive consent documents that meet ethical and regulatory
standards, and how to effectively communicate study information to participants. Attendees
will gain a deep understanding of the informed consent requirements, and practical
strategies for fostering trust and transparency with study participants. This training
is ideal for researchers seeking to improve their consent process and ensure compliance
with federal regulations.
Training will be recorded and available for viewing |
Managing Modifications, Incident Reports, and Closures in Cayuse
Wednesday, October 8, 2025
1:00 p.m.
In this training session, participants will learn the essential procedures for managing
study modifications, incident reports, and closures using the Cayuse IRB system. This
interactive session will cover how to effectively submit modifications when changes
occur in a study protocol, report incidents that may impact the safety or integrity
of the research, and formally close a study upon completion. Attendees will learn
how to navigate through Cayuse, ensuring compliance with IRB requirements, and understanding
best practices for maintaining accurate documentation throughout the research lifecycle.
This training is ideal for researchers, coordinators, and administrators involved
in IRB submissions.
Training will be recorded and available for viewing
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Recruitment and Compensation in Human Subjects Research: Ethical and Regulatory Considerations
Monday, October 20, 2025
11:00 a.m.
This training session provides researchers with essential guidance on the ethical
and regulatory frameworks governing recruitment and compensation practices in human
subjects research. Participants will learn how to design recruitment strategies that
are equitable, non-coercive, and compliant with federal and institutional standards.
The session will also address appropriate methods for compensating participants without
exerting undue influence, and will explore special considerations for vulnerable populations.
By the end of the training, attendees will be equipped to implement ethically sound
practices that respect participant autonomy and promote trust in the research process.
Training will be recorded and available for viewing
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Ethical Management of Study Data
Tuesday, November 4, 2025
1:00 p.m.
This training session will explore the ethical responsibilities researchers hold in
collecting, storing, analyzing, and sharing study data. Participants will gain a clear
understanding of best practices for maintaining data integrity, ensuring confidentiality,
and meeting compliance standards.
Training will be recorded and available for viewing
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IRB Compliance: Avoiding Common Pitfalls
Wednesday, November 19, 2025
12:00 p.m.
A session that highlights frequent mistakes researchers make in IRB submissions and
compliance, offering strategies for avoiding delays.
Training will be recorded and available for viewing
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