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Hear straight from the experts that executed rapid study start-up and study management using a ‘no touch’ protocol while under quarantine, stay at home orders. The panel will share their real-world experience on rapid study deployment and lessons learned in developing and initiating two large randomized clinical trials studying the effects of hydroxychloroquine in outpatients with confirmed COVID-19 in under two weeks.
Learning Objectives:
Describe resources for rapid deployment of emergency IRB review, eConsent, and DSMB review.
Demonstrate how to direct a high performing team and develop a quality risk assessment.
Identify database build requirements and collaboration with RCs, CRAs and Research Nurses.
Speaker(s):
Jeri
Burr,
RN,
Executive Director,
University of Utah
Nina
Pacchia,
PhD, CCRC,
Program Director,
University of Utah
Sam
Sorenson,
BS, CCRC,
Project Manager III,
University of Utah
Credits
1.00
- ACRP Credits
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