Training Calendar

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 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 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.

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