“Informed Consent for Vulnerable Populations in Clinical Research: Balancing Protection, Access, and Equity”
Clinical Research Investigator Seminar Series
April 25, 2025
12:00 PM - 1:00 PM
Location
Virtual via Zoom
Calendar
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Description:
This talk explores the ethical and regulatory challenges of obtaining informed consent from vulnerable populations in clinical trials. It will discuss strategies to ensure ethical enrollment while balancing the need for scientific rigor, equitable access to research, and participant protection. Attendees will gain insights into regulatory frameworks, risk-benefit considerations, and best practices for fostering inclusivity in clinical research.
Speakers:
Ryan Nguyen, DO
Assistant Professor of Clinical Medicine
Precision Oncology Program Lead
&
Meredith Russell, BS, CCRP
Associate Director of Clinical Research Operations, Clinical Trials Office
University of Illinois Cancer Center
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
Feb 12, 2025
Date updated
Feb 12, 2025