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.

Contact: Sudeshna De, Lawrie Zhang, ccts-training@uic.edu