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IRB Topical Workshop: The IRB and Qualitative Research

Register for this workshopThis online session will help researchers using qualitative methods design participant-centered research and communicate their qualitative research endeavors to the IRB. We will cover:Research approaches: phenomenology, grounded theory, case study, ethnography, autoethnography, and narrative inquiryResearch data collection modes: interviews, focus groups, observations, photovoice, and surveysRisks to primary and third party participants and…

IRB Topical Workshop: Using “Apps,” Software, and Wearables in Research with Human Subjects

Register for this workshopThis online session will discuss the use of “off the shelf” apps and software and “homegrown” apps and software when used in research with human subjects.Attendees in this session will learn about and discuss:How to describe the app/software when used as a tool for data collectionHow to describe the app/software when it’s…

IRB Basics Part I: An Introduction to the IRB process at NC State

Register for this workshopThis online workshop provides a basic overview of IRB history and operations. It is designed for individuals with little to no background in human subjects research practices at NC State University and serves as a foundation for all other IRB workshops offered through the NC State University Libraries, including the IRB Basics:…

RA Training Series: E-Retroactive Adjustment Form (RAF) Process Update Training

Zoom join link:https://ncsu.zoom.us/j/91943209418The Research Education and Training Team proudly hosts this live training opportunity. Beginning March 1, the Office of Contracts and Grants will transition submission and review of over 90-Day HR cost transfer actions to the new E-Retroactive Adjustment Form (RAF) process. After this date, submissions will no longer be accepted via redistribution@ncsu.edu. Come to…

IRB Basics Part III: eIRB Application Workshop

Register for this workshopThis online session will go through the eIRB application question-by-question and provide targeted guidance for how to fill the application out and how to upload supporting documentation and what documents to upload. This session will focus on how to fill out the eIRB application for qualitative, quantitative, and clinical trials research; biomedical…

IRB Basics Part II: Handling Your Data and Assessing Risks & Benefits

Register for this workshopThis online workshop discusses data management and risks/benefits ratios in human subjects research and further guidance on how to communicate those in your IRB application. Participants must have completed IRB Basics: Part 1 to attend.Instructor: Yael Allen