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Clinical Trials Training for Investigators & Coordinators (CTTIC)

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

 CTTIC Training Descriptions

 

CTT 101 - Clinical Trial Core Training

  • This 8 hour training will provide a broad overview of how clinical trials are conducted.  The first part of this training is ON-LINE and will take approximately 4 hours to complete.  It can be taken over a period of days if needed, however it must be completed before the INSTRUCTOR-LED training in class.  Some of the topics of the on-line training will include: Terminology and References, Drug and Development Process, and Device Development.  The instructor led training will take an additional 4 hours.  Some of the topics of the instructor led training will include: Trial Design, Clinical Trial Conduct, and Roles & Responsibilities.   

    • CTT 102a - Submitting to COMIRB (Session 1)*

  • 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. 

    • CTT 102b - Submitting to COMIRB (Session 2)

  • This 1.5 hour training will provide an introduction to the ongoing reporting requirements such as the continuing review form and the unanticipated problem form. 
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    CTT 103 - Submitting to IBC*

  • This 1 hour training will cover human gene transfer and the NIH guidelines to performing this type of research. 
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    CTT 104 - Budgeting for Clinical Trials**

  • This 2 hour training will go over steps on creating the budget template, thinking through what needs to be included, and how to check for overlooked items. 
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    CTT 104 - Budgeting for Clinical Trials ONLINE COURSE

    • Access to Course:
      FOR UNIVERSITY EMPLOYEES:  Login to your MyCU portal page at https://my.cu.edu/, then click on the MY.TRAINING tab. Click on Click here for SkillPort-CU’s Online Learning. Click on the CU Learning Programs option in the left side Shortcuts menu. Locate the course titled, CU: Budgeting for Clinical Trials. After clicking the course title a second time, click Play to begin the course and the quiz. **Access to SkillPort is provided ONLY through your log-in to your personal "MyCU Portal" page. If you have trouble, please first reference the helpful documents at the Employee Learning and Development website, Resources page, at: https://www.cu.edu/content/resources.**
      FOR NON UNIVERSITY EMPLOYEES: If you cannot access the portal with your sign on information, contact Nicole Ganley

    CTT 105 - Writing Informed Consents

  • 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. 

    • CTT 106 - Recruitment for Clinical Trials

  • 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. 

    • CTT 107 - Preparing for FDA Audits

  • 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.
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     All trainings are offered in class.

    *Trainings will be offered in a video format in the future.

    **Training is being currently offered year around through the My CU portal in the UC Skillport Online Learning System.