Clinical Trials Research Coordinators

 

Training and Education

Federal requirements for education in the protection of human research participants are met according to Colorado Multiple Institutional Review Board (COMIRB) policy for all affiliated/local principal investigators, co-investigators, and research coordinators listed on human research protocols by successfully completing the CITI course in human subject protections and the Conflict of Interest (COI) prior to submitting a protocol.

 

Woman sitting at computer

Optional Clinical ResearchTraining
Office of Regulatory Compliance Training Calendar

 

Clinical Trials Training for Investigators and Coordinators is provided for study coordinators and investigators conducting clinical research and covers:

  • Clinical trial core training
  • Submitting to COMIRB and unanticipated problems
  • Submitting to Institutional Bio-Safety Committee (IBC)
  • Budgeting for a clinical trial
  • Informed consent for clinical trials
  • Recruitment for clinical trials
  • FDA audits



  • The CITI Good Clinical Practice Course is designed specifically for clinical researchers participating in human subjects research to have knowledge of:

    • Federal regulations
    • International Conference on Harmonisation (ICH)
    • Regulations and good clinical practice guidelines