Training Calendar

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

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

In this course, attendees will observe the correct methods for obtaining height, weight, and vital signs (blood pressure, temperature, pulse, and respirations) from ADULT patients. Attendees can also participate in a walking tour of the CTRC clinic.

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.

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