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Implementation of eConsent and Other Digital Clinical Trial Innovations
Session Chair(s)
Cassandra Smith, MBA
Director, Diversity, Equity, and Inclusion in Clinical Trials, Janssen Research & Development, United States
Learn about using eConsent in the informed consent process. Insight will be shared into understanding how eConsent may be used to improve the consent process; how this may impact sites, IRBs, and sponsors; and how the use of eConsent may impact the patient experience. Finally, attendees will learn how to use other digital tech innovations to advance patient centricities.
Learning Objective : Describe how eConsent may be used to improve the entire consent process including the improving the patient experience in clinical trials; Discuss available resources to support implementation of eConsent for sites, IRBs, and sponsors; Analyze findings from surveys and pilots to understand eConsent experience; Explain how data platforms are supporting stakeholders flexibility to advance patient centricity powered digital tech innovations, accelerate study design, and improve data quality.
Speaker(s)
Cassandra Smith, MBA
Director, Diversity, Equity, and Inclusion in Clinical Trials, Janssen Research & Development, United States
Transforming Informed Consent: Current Landscape and Tools to Enable the Future of eConsent
MaryAnne Rizk, PHD
Head, Life Sciences Clinical Strategy, AWS, Amazon, United States
Driving Clinical Outsourcing Innovation Forward with Machine Learning: Self-Driving Systems to Automate and Accelerate
Eric Delente, MA
Consultant, Self-employed, United States
eConsent: A Patient-Centric Program to Improve Enrollment, Recruitment, and Retention
Cami Gearhart, JD
CEO, Quorum Review IRB, United States
Are Your Sites Prepared for eConsent?
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