Veeva SiteVault Best Practices: Join fellow SiteVault peers as they share proven strategies from the front lines of research. Leaders from Boston Children’s Hospital, the University of Pennsylvania, and Geisinger Health system will share the processes and tools they use to make their ISF management efficient, and how they leverage SiteVault as a tool to scale research capacity. Attendees will explore critical features, adoption strategies and best practices to keep their site ahead of the curve for tomorrow’s trials, and leave with tangible recommendations and peer connections to carry through the rest of Summit and beyond.
Step into the design process and directly influence the future of sponsor-provided technology. Participants will provide real-time feedback on current product experience and evaluate early-stage designs spanning the entire trial lifecycle—from initial feasibility to final study archival — all while enjoying a casual lunch with site and sponsor peers.
By sharing your front-line experience, you will help develop Veeva solutions to enable seamless site-sponsor collaboration for tomorrow.
By sharing your front-line experience, you will help develop Veeva solutions to enable seamless site-sponsor collaboration for tomorrow.
Join site, sponsor and CRO leaders in a hands-on, collaborative workshop focused on shifting site and sponsor engagements from study-by-study transactions to long-term strategic alliances. From feasibility to data exchange, cross functional teams of sites, sponsors and CROs will partner to tackle challenges throughout the study lifecycle.
Through interactive discussions and fast-pasted presentations, participants will design actionable frameworks that make sites and their sponsors more efficient, learn from each other, and expand their networks along the way.
Through interactive discussions and fast-pasted presentations, participants will design actionable frameworks that make sites and their sponsors more efficient, learn from each other, and expand their networks along the way.
Kick off Summit at a dedicated happy hour focused on bringing the research site community together. Connect with peers and celebrate ahead of the welcome reception!
Day 1
Join the Veeva Site Advisory Council (SAC) as they share this year’s survey results and case studies. Council members will lead interactive discussions on the findings and explore the path forward to improve the site experience.
Hear from principal investigators as they share lessons learned from leading clinical research and their perspectives on the future of site participation and clinical trials.
Discover how Veeva SiteVault’s unified platform has created a connected core framework for site business operations, sponsor integration, and intelligent automation.
Learn how today’s legislative landscape impacts technology adoption, clinical trial funding, and the future of real-time clinical trials.
Day 2
Enjoy your morning breakfast while walking through a Site’s day in the life. This interactive demo session will highlight end to end workflows in SiteVault and other Veeva tools, with emphasis on improving efficiencies between sites and sponsors.
Preview Veeva eSource’s next-generation capabilities, including CRF generation, EHR integration, and how direct streaming to EDC will simplify data flow from sites to sponsors.
Drop in and meet sponsors that align with your therapeutic areas, patient populations, or studies of interest. This is dedicated time to bring sponsors and sites together and make matches that can lead to new partnerships.
Hear from Research Sites on how they have overcome operational and technology challenges, or led unique innovations.
SiteVault customers describe their experiences adopting unified site technology. Learn how it has improved site operations and their approach to successful implementation.
Hear directly from sponsors as they share their perspectives on site training, feasibility, and payments, along with the initiatives they’ve implemented to strengthen site partnerships.
Preview Veeva eSource’s next-generation capabilities, including CRF generation, EHR integration, and direct streaming to EDC will simplify data flow from sites to sponsors.
Explore how patient advocacy is shaping clinical research by influencing trial design, participant engagement, and collaboration across the clinical research ecosystem.