Informed Consent for Vulnerable Populations in Clinical Research: Balancing
CCTS Training and Advancement of Careers in Translational Science (TrACTS)
April 25, 2025
12:00 PM - 1:00 PM America/Chicago
Location
Virtual via Zoom
Calendar
Download iCal FileSpeakers
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
About this Talk
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.
About the Series
CRISS seminars are 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
Apr 3, 2025
Date updated
Apr 3, 2025