Clinical Trials Training for Investigators & Coordinators (CTTIC)

This is a continuation of the 4 hour course broken into two sessions. Students will learn about the continuing review form and how to report unanticipated problems  This course is free.

This 2 hour course will go over the steps involved in preparing a budget template.  You will learn how to create the template, think through what to include, and how to check for overlooked items.  This is the face-to-face version of the on-line course.  If you do not want to take the on-line version, you can come and learn directly from one of the creators of the on-line course.  This course is free.

In this 2 hour course, we’ll go over the steps involved in recruitment and provide tips based on the experience of the presenters, national studies that have had a high take-up and retention rate, the regulations surrounding recruitment.  We will also include a section on recruiting protected and special populations.  Snacks will be provided.  This course is free.

This 8 hour training will provide a broad overview of how clinical trials are conducted.  Some of the topics covered include: Terminology and References, Drug and Development Process, Roles and Responsibilites of coordinators and investigators.

This 3 hour training will go over considerations and regulations for the entire consent process.  Participants will also learn how to write consents at reading levels below 8th grade and how to check for missing pieces.

This 1.5 hour training will introduce you to the ongoing reporting requirements required by COMIRB such as the continuing review form and the unanticipated problem form.

This 8 hour training consists of a 4 hour online and 4 hour in-class training.  The online component will need to be completed before the in-class training.  Instructions explaining how to take the online component will be sent from the Colorado Prevention Center one month before the in-class training.  This full training will provide a broad overview of how clinical trials are conducted.  Some of the topics covered include: Terminology and References, Drug and Development Process, Roles and Responsibilites of coordinators and investigators.

This 2 hour training will go over the steps involved in recruitment, national studies that have had a high take-up and retention rate, and the regulations surrounding recruitment.  Also included will be a section on recruiting  protected and special populations.

This 2 hour training will cover what is to be expected during an FDA audit, how to follow up, 483 citations, and lessons learned by others who have gone through audits.

This 2.5 hour training will provide an introduction to human subjects research and the differences between Exempt, Expedited, and Full Board reviews.  Participants will also learn the step by step guide to filling out the COMIRB application and the appendices. 

This 8 hour training will provide a broad overview of how clinical trials are conducted.  Some of the topics covered include: Terminology and References, Drug and Development Process, Roles and Responsibilites of coordinators and investigators.

This 2 hour training will go over the steps involved in recruitment, national studies that have had a high take-up and retention rate, and the regulations surrounding recruitment.  Also included will be a section on recruiting  protected and special populations.