“After IRB Approval…Keeping Your Study Compliant”
Clinical Research Investigator Seminar Series
March 28, 2025
12:00 PM - 1:00 PM
Location
Virtual via Zoom
Calendar
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Description:
What investigators need to know and how to prepare when their study is selected for monitoring. Review and discussion of the Clinical & Human Subject Research Compliance program’s purpose and process to assist investigators in maintaining study compliance.
Speakers:
Erin Vidra, MS, CHRC
Director, Clinical & Human Subject Research Compliance
Office of Vice Chancellor for Research
University of Illinois Chicago
&
Erin (EJ) Jaworski, MPH, CHES
Clinical Research Compliance Specialist
Office of the Vice Chancellor for Research
University of Illinois Chicago
Clinical Research Investigators Seminar Series (CRISS): This training seminar series is intended to provide faculty and other investigators with information and skills needed to conduct clinical research at UIC at all stages of a study’s lifecycle.
Date posted
Jan 9, 2025
Date updated
Mar 11, 2025