About this Event
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Part of the Helen Diller Family Comprehensive Cancer Center (HDFCCC) K12 Program's Concept to Completion, Strategies for Successful Clinical Trials Seminar Series, that aims to provide high-yield, practical information about designing, funding, and conducting patient-facing oncology trials.
Speakers:
- Katie Kelley, MD - UCSF Professor of Clinical Medicine, Department of Medicine (Hematology/Oncology)
- Alan Venook, MD - UCSF Professor of Medicine, Department of Medicine (Hematology/Oncology)
- John McAdams, MS, CCRP - HDFCCC Director, Data and Safety Monitoring Committee
- Edward Kuczynski - Director, UCSF Human Research Protection Program (HRPP)
Learning Objectives:
- Review clinical trial ethics
- Explain the HDFCCC informed consent training process
- Describe the role of the IRB
UCSF promotes the exchange of diverse ideas and perspectives, acknowledging that the views and opinions of our guest speakers on campus are their own and may not reflect the perspective of the University. We embrace free speech in the pursuit of greater understanding, consistent with our obligations as a public university under the First Amendment.
