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About This Webinar

As clinical trials grow more complex, study teams face increasing challenges in managing data quality, integration, and regulatory compliance. The use of AI and machine learning (ML) is transforming how clinical data is collected, analyzed, and acted upon, enabling more efficient and insightful trial management.

This webinar will explore how AI enhance data surveillance, improve data quality, and streamline integration to enable actionable insights. Experts will discuss practical approaches to meeting regulatory requirements while optimizing trial execution. Through real-world case studies, attendees will gain insights into how these technologies and CRO expertise address common pain points, reduce risks, and improve overall study outcomes.

Agenda
  • How AI enhances data surveillance, quality, and integration for actionable insights
  • Practical approaches to meeting regulatory requirements while optimizing trial execution
  • Real-world case studies showcasing how AI and CRO expertise: Address common pain points , reduce risks and Improve overall study outcomes
When: Monday, June 23, 2025 · 6:00 p.m. · Jerusalem
Duration: 1 hour
Language: English
Who can attend? Everyone
Dial-in available? (listen only): No
Featured Presenters
Webinar hosting presenter
Senior Vice President, Data Experience, Medidata
Wayne is Senior Vice President, Data Experience (including Rave EDC, Medidata Clinical Data Studio, Medidata Designer, Rave Imaging, Rave RTSM, Rave Coder+, and Rave Safety Gateway) at Medidata. His responsibilities include the strategy, development, and delivery of these products across all Research & Development disciplines. Before joining Medidata, Wayne spent 12 years overseeing Product Management for clinical technology used by Data Management and Biometrics at PRA Health Sciences, which included oversight of Platform as a Service, Software as a Service, on-premise deployed environments, and in-house developed solutions.
Webinar hosting presenter
Chief Data Strategist & Solutions Officer, Bioforum The Data Masters
As a certified clinical data manager, Tanya holds a M.Med.Sc. in Hematology and Cell Biology from University of the Free State, as well as her project management professional certification. She has vast industry experience with over 14 years with IQVIA (legacy Quintiles). As manager of various data management operation teams, Tanya has actively led strategies for customized data delivery solutions focusing on timely quality data. She has driven numerous innovation teams, and her dedication to optimal customer service/delivery is visible through her long-standing relationships.
Webinar hosting presenter
Senior Director, Product Marketing, Data Experience, Medidata
Andy Gurd is a Senior Director of Product Marketing at Medidata, where he is responsible for product marketing strategy, messaging, and content for the Medidata Data Experience, which includes Medidata Clinical Data Studio. Andy has over 25 years of technology product marketing experience, the last 11 of which have been working with clinical research technologies and services, including 6 years with Parexel. Before entering life sciences, Andy spent 13 years in product marketing/management roles for systems and software engineering technologies, including 5 years with IBM.