Adverse Experience Assessment in Clinical Trials
Clinical Research Investigator Seminar Series
January 23, 2026
12:00 PM - 1:00 PM
Calendar
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This session will discuss the role of the investigator in assessing adverse experiences occurring during clinical trials, and how investigator assessments are integral to identifying adverse requiring expedited safety reporting.
Speaker:
Natalie Reizine, MD
Assistant Professor of Medicine
Department of Medicine, Division of Hematology and Oncology
University of Illinois College of Medicine Chicago
Assistant Professor of Medicine
Department of Medicine, Division of Hematology and Oncology
University of Illinois College of Medicine 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
Dec 9, 2025
Date updated
Dec 17, 2025