Skip to main content
CCTSI

Training & Education

Go Search
Home
About Us
CTRC
Research Resources
Training & Education
Community Translation
Funding Opportunities
Child & Maternal Health
Contact Us
  

Home > Training & Education > Clinical Trials Training for Investigators & Coordinators (CTTIC)
 
Clinical Trials Training for Investigators & Coordinators (CTTIC)

 About the Program

ClassroomThe Clinical Trials Training for Investigators and Coordinators (CTTIC) is designed to provide specialized training to research study coordinators and investigators.  It consists of 24 hours of content and is delivered by staff at UCDHSC and affiliated institutions.  While the curriculum is aimed at new investigators and coordinators, it may be recommended for investigators who are experiencing problems with COMIRB review, writing consent forms, protocol violations, or patient safety issues. 

 CLINICAL TRIALS CURRICULUM TOPICS INCLUDE:

  • CTT 101 - Clinical Trial Core Training
  • CTT 102 - Submitting to Colorado Multiple Institutional Review Board (COMIRB)
  • CTT 103 - Submitting to Institutional Bio-Safety Committee (IBC)
  • CTT 104 - Budgeting for Clinical Trials
  • CTT 105 - Writing Informed Consents
  • CTT 106 - Recruitment for Clinical Trials
  • CTT 107 - Preparing for FDA Audits

An individual may take one or more of the trainings as many times as they feel appropriate in no particular order. 

    You must be a member to utilize ETCD resources, apply for funding opportunities, and attend events. To become a member, please visit our membership page.  Membership is free.
 
 

 CTTIC Announcements

Registration for January 2010 trainings NOW OPENUse SHIFT+ENTER to open the menu (new window).
CLINICAL TRIAL CORE TRAINING CHANGES Use SHIFT+ENTER to open the menu (new window).

 Training Materials

Listed below are samples of the powerpoints used during in-person trainings.

 Useful Links

  Colorado Multiple Institutional Review Board (COMIRB)
  Colorado Prevention Center
  Institutional Biosafety Committee
  Genetic Modification Clinical Research Information System (GeMCRIS)
  NIH Guidelines for Research Involving Recombinant DNA Molecules
  NIH-Office of Biotechnology Activities
  Recombinant Advisory Committee
  RegSource Regulatory
  U.S. Food and Drug Administration

 CTTIC Contacts

For more information contact: Yvonne Kellar-Guenther, PhD or Nicole Ganley, 720.848.6663.