Training Calendar

In this training, participants will learn step-by-step instructions for filling out the COMIRB application and the attachments.

This course will take the student through the step-by-step process of obtaining subject informed consent.

This lecture provides an overview of protocol writing and development for investigators conducting human subject research. Topics covered include protocol purpose, audience-appropriate communication through writing, scientific design, and protocol organization with a content discussion of each protocol section.

This course will provide an overview of the ClinicalTrials.gov system including the requirements for posting a trial, common mistakes when posting and continuing responsibilities.

This training will cover the steps involved in recruitment, discuss national studies that have had high enrollment and retention rates, and the regulations surrounding recruitment.

This training will provide an introduction to human subjects research regulations; the differences between Exempt, Expedited, and Full Board reviews; and an introduction to human subject research involving vulnerable populations.

This course will discuss the PI's additional responsibilities when COMIRB is serving as sIRB, explain the process and procedures for COMIRB, the PI, and the relying sites, and explain when and how the Smart IRB network is used for this purpose.

This course will take the student through the step-by-step process of obtaining subject informed consent.