Today’s clinical trial landscape requires the use of various patient technology solutions to support participant enrollment and the collection, management and review of clinical data, which ultimately informs clinical decisions and trial results. In order to improve data quality, optimize workflows and create a seamless end-user experience, it’s important to leverage the appropriate clinical technology strategy.
In this webinar, industry experts will explore how best-in-class clinical technology solutions can be used independently to optimize clinical trials and when/how these technologies can work together to create further workflow benefits. In this session, they will discuss how to:
- Design and execute a patient technology strategy that fits unique study needs
- Reduce clinical site burden by streamlining processes across eConsent, interactive response technology (IRT) and electronic clinical outcome assessment (eCOA)
- Quickly leverage insights collected from patient data to improve compliance, study optimization and decision making
Register for this webinar to learn how to effectively implement patient technology strategies that streamline data collection and improve study compliance.
Speaker
Anthony Mikulaschek, Vice President, Commercialization, IQVIA Patient Suite
As Vice President of Commercialization for the Patient Suite at IQVIA, Anthony Mikulaschek is responsible for the commercialization of IQVIA’s eCOA, eConsent and IRT platforms. This includes pricing and sales strategies, opportunity configuration, market needs review, IQVIA technology market placement and strategy. Anthony has extensive experience in validated system configuration, implementation, systems integration, business process reengineering, IT operations and consulting. He has successfully led the development, delivery and management of technology solutions for over 37 years, including 29 years in the pharmaceutical sector.
Message PresenterWho Should Attend?
This webinar will appeal to Managers, Directors, VPs and C-suite level clinical research professionals in large to mid-size pharma companies, particularly those in the following departments:
- Clinical Operations
- Clinical Development
- Clinical Monitoring
- Clinical IT
What You Will Learn
Attendees will learn how to:
- Design and execute a patient technology strategy that fits a clinical trial’s unique needs
- Reduce clinical site burden by streamlining processes across eConsent, IRT and eCOA
- Leverage insights from patient data quickly to improve compliance, study optimization and decision making
Xtalks Partner
IQVIA
IQVIA (NYSE:IQV) is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry. IQVIA creates intelligent connections to deliver powerful insights with speed and agility — enabling customers to accelerate the clinical development and commercialization of innovative medical treatments that improve healthcare outcomes for patients. With approximately 82,000 employees, IQVIA conducts operations in more than 100 countries. Learn more at www.iqvia.com.
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