From Concept to Execution – Designing & Executing Patient and Site-Centric Trials Workshop at Medidata NEXT NY

Please join us before Medidata NEXT NY kicks off for an interactive hands-on workshop creating protocols that prioritize both patients and sites. Join your peers for an engaging, interactive experience designed to provide you with actionable insights and practical knowledge to achieve successful clinical trials.

Today’s clinical trials demand solutions that enhance – not complicate – the trial experience for patients and sites. When thoughtfully applied, technology, data, and AI can work together to reduce burden, improve efficiency, and increase the probability of trial success.

Join us for an engaging, interactive afternoon—with a touch of friendly competition!—as we collaborate across roles to design a protocol that enhances the experience for both patients and sites while optimizing trial efficiency. Through team-based activities and hands-on exercises, you’ll gain practical insights into how Medidata’s solutions create streamlined, impactful trials geared toward optimal outcomes.

Key Takeaways:

• Understand how AI can help you leverage insights from historical, cross-sponsor trial data to select the best sites, patient populations, and endpoints.
• See how a patient-centered suite of technologies enables seamless data and workflows, enhancing trial operations from recruitment to post-trial follow-up.
• Explore the integration of eCOA and sensor activities into a single patient portal, achieving efficient workflows, holistic patient insights, and high endpoint quality.

Who Should Attend:

• Clinical Development professionals responsible for designing study protocols – including defining endpoints, identifying patient populations, determining trial size, and ensuring protocols are designed to gather proper evidence to meet regulatory and scientific standards.
• Clinical Operations leaders tasked with trial oversight, including managing timelines and site relationships to ensure trials run efficiently and with minimal disruptions to patients and sites.
• Clinical Innovation experts working to integrate AI, predictive analytics, and digital solutions into clinical trials to improve protocol design and streamline clinical and operational workflows for both patients and sites.
• Chief Medical Officers and Therapeutic Area Leads who set clinical strategy and provide oversight for trial protocols, focusing on aligning therapeutic goals with patient- and site-friendly approaches to maximize trial success.
• Heads of Data Management focused on implementing data collection and monitoring systems that improve data quality, streamline patient reporting, and reduce burdens on trial sites.
• Site and Patient Management professionals responsible for maintaining site relationships, engaging patients, and ensuring both groups are supported with technology that simplifies participation and enhances experience.