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.
Speakers
Melissa Mooney, Director, Solutions Engineering, IQVIA Patient Suite
Melissa Mooney has over 19 years of experience in the development of eCOA solutions for use in clinical trials. Melissa’s area of expertise is eCOA solution design where she has supported clients and eCOA vendors in developing robust and usable eCOA software solutions that meet eCOA protocol requirements. She also brings a plethora of experience in eCOA requirement gathering, leading eCOA User Acceptance testing, eCOA data management, and BD support.
Message Presenter
Chris Driver, Senior Director, Product Management, IQVIA Patient Suite
With over two decades in the clinical technology space, Chris brings a wealth of expertise across Product, R&D and Information Technology functions. Chris leverages a deep understanding of the sponsor, site, and patient experience to drive innovation and excellence in clinical research solutions. With a particular focus on product innovation and the development of global health platforms, Chris’s passion for innovative healthcare technology is driven by a vision for a future where patient care is both personalized and accessible. Outside of his professional endeavors, Chris enjoys spending time with his growing family, and advocating for adoption, particularly for children blessed with an extra chromosome.
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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