Description:

Informed Consent & Questionnaires of Non-English Speaking Participants and Special Populations

This seminar will cover the policy, regulatory requirements, and patient facing aspects of consenting non-English speaking patients.

Speaker: 
Rachel Olech 
Senior Regulatory Specialist, CCTS

&

Meredith Russell
Associate Director of Clinical Research Operations
Clinical Trials Office, UI Cancer Center

RC+ Program:
Core Competency #2: Ethical and Participant Safety Considerations

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