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Using Big Data to Design Smarter Studies
Session Chair(s)
Jane Elizabeth Myles, MSc
Program Director
Decentralized Trials and Research Alliance (DTRA), United States
Smart Patients Build Smart Protocols: Putting the Patient’s Voice into Your Design
Learning Objective : Define the guiding principles and outlines of a process for optimizing study design for more efficient execution (and ensuring appropriate data capture); Describe the role information integration and scenario planning play in good design practices; Explain some of the challenges and successes in using EHR data, structured design information, and patient input to design studies.
Speaker(s)
Smart Patients Build Smart Protocols: Putting the Patient’s Voice into Your Design
Jane Elizabeth Myles, MSc
Decentralized Trials and Research Alliance (DTRA), United States
Program Director
Innovative Solutions to Program Design: Using a Computer-assisted Design Platform to Drive Quality in Design
Rick Sax, DrMed, FACP
Pharma Design Solutions, Ltd., United Kingdom
Managing Director
Optimizing Study Design for Efficient Trial Execution
Igor Gary Altman
Medidata Solutions Worldwide, United States
Senior Director, Product Management
Using the Right Tool for the Right Job: Methods for Gaining Patient Input into Protocol Design
James Kremidas
Wake Forest Clinical Research, United States
Adjunct Graduate Faculty Member
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