Research Staff Training

Overview

It is the investigator’s responsibility to ensure that all research personnel are trained appropriately and in a timely manner for all aspects of the clinical trial for which they are accountable. Training may include, but is not limited to, the following topics:

  • Subject consent
  • Data collection, maintenance and storage
  • Regulatory reporting
  • Drug dispensing, accountability, and destruction
  • Intervention/Interaction procedures
  • Management and reporting of Adverse Events (AE), Serious Adverse Events (SAE), Unanticipated Adverse Device Effects (UADE), and Unanticipated Problems (UaP), and other reportable occurrences

It is important to provide documentation that training has been provided. Standard Practice Guidelines for the documentation of the training might include the use of training logs or agendas. It is also important to maintain the appropriate level of training throughout the course of the clinical trial in order to accommodate changes in the protocol, work process, and the use of new equipment or technology.

Related Resources

Program for Education and Evaluation in Responsible Research and Scholarship - PEERRS

HRPP Operations Manual (OM)  

Standard Practice Guideline (SPG) Templates for Clinical Trials (link to page w/complete list of downloads)

Downloadable Templates and Appendices

Research Staff Training.docx

Questions?

Contact us at MICHR-SPGSupport@umich.edu.

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