The urgency to revolutionize the process by which sponsors assess a study site's feasibility for handling a clinical trials has never been more apparent. This session considers how, as trial volumes surge and staffing shortages loom, the frustrations shared by sponsors, contract research organizations (CROs), and sites alike underscore the need for innovative approaches to data collection and site selection that will lead to successful trials.
CEU: 1.00 ACRP
Speakers:
Andrea Bastek, PhD, VP of Innovation, Florence Healthcare
Amy Bland, Director of Clinical Research, Baptist Health Institute for Research and Innovation
Victor Chen, Managing Director, Clinical Trials Program, Kaiser Permanente
Nancy Sacco, PhD, VP Head of Clinical and Site Development Operations, SiteBridge Research Inc
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