Wednesday May 22, 2024
12:00 PM – 1:00 PM
Speakers: Christina Smith and Charles Robinson
UNC Office of Clinical Research Compliance
Christina Smith is the Director of Clinical Research Informatics in the UNC Office of the Vice Chancellor for Research, where she oversees support for OnCore, Veeva SiteVault and eConsent, and REDCap. Previously, she held positions at Duke’s Clinical and Translational Science Institute, Cornell University, the Center for Medicare and Medicaid Innovation, and the American Urological Association. Healthcare is Christina’s second career: she spent more than 10 years in science communications in Washington, D.C., providing executive speechwriting, science writing, public relations, and committee support to several large scientific associations. She is a registered nurse, with a BSN from the University of Maryland, Baltimore, and an MHA from the UNC Gillings School of Global Public Health.
Charles Robinson is the Veeva Application Administrator in Clinical Research Informatics. He has 10 years of experience working with local government; implementing software, performing business analysis, and integrating systems. Before that, he spent 10 years working in higher education at the University of Nevada, Reno.
Objectives:
- To understand how to set up a study eBinder and manage documents
- To understand how Study Connect works between sponsors and sites
- To understand how to manage eConsents
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