Title: NRP February 2025 Education Session (Rescheduled from Feb 19): The Informed Consent Process: Why It Matters and How to Get It Right
Presented by Brett Phillips, MA, PMP, CCRP Clinical Research Program Manager for the UNC Blood Research Center
Former study coordinator and current hematology research program manager. 10+ years of experience consenting research participants in oncology and hematology in phase II-IV drug studies including gene therapy.
Objectives:
By the end of this session, study coordinators will be able to:
- Recognize the historical and ethical significance of informed consent in clinical research.
- Prepare effectively before obtaining consent to improve participant understanding and engagement.
- Handle difficult consent conversations with confidence and professionalism.
- Implement post-consent best practices to strengthen study integrity and participant trust.
The session will be hybrid.
In-person will be in Rm 219, Brinkhous-Bullitt Bldg. (2nd Floor) within NC TraCS Institute and lunch will be provided to those registered for in-person.
Virtual : Zoom link is included in the registration confirmation for live virtual viewing.
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"View my Registration". Find the registration you want to edit and click “edit” at the far right.