Training Calendar

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.

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.

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.