University Research Training Calendar
Clinical Research Support
Colorado Multiple Institutional Review Board
Conflict of Interest
Environmental Health & Safety
Office of Grants and Contracts
Office of Laboratory Animal Resources
Office of Research Committee Support
Clinical Trial Coordinators
This courses provides an overview of 2 CFR 200 (Uniform Guidance) by reviewing the provisions most applicable to research administrators at the University.
This course provides an overview of the day-to-day aspects of a pre-award research administrator
This training will introduce the learner to the process of developing a budget for a clinical trial.
This course will provide the participant with a practical understanding of what to expect before, during, and after an FDA audit.
This course will take the student through the step-by-step process of obtaining subject informed consent.
The workshop guides learners through the development of key sections of a human subject research protocol. Through homework assignments, learners should have a completed protocol ready for SARC and/or COMIRB submission by the end of the series.
Do you want to know how UCHealth upholds federal regulations regarding human participant research? Come learn about and discuss UCHealth’s research-related policies!