Cedars-Sinai
Los Angeles, CA
Geneva Williams, CIP, is the Manager of IRB Operations in the Office of Research Compliance & Quality Improvement at Cedars-Sinai. She has been with the department since 2011 and oversees the administrative functions of the IRB submission, review, and approval process. Geneva has presented on various research compliance topics such as informed consent, stem cell research ethics and oversight, and requirements for conducting research with drugs and medical devices.
B25 - [IN-PERSON ONLY] Institutional Review: What HRPPs and IACUCs Can Learn from Each Other
Monday, December 4, 2023
2:15 PM – 3:15 PM ET