Veeva Connect is now available to watch Summit content on demand.
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You’re invited to watch sessions curated by clinical data management experts from life sciences companies.

Veeva Connect is your connection to the people, the know-how, and the innovation that Veeva shares at Summit — all year around.

Below, you’ll find a taste of Summit with highlights from the clinical data management track.

Learn more and view the full agenda here

Featured Clinical Data Management Sessions

You have on demand access to dedicated clinical data management sessions. Featured customer-led sessions include:


GSK shares its strategy for modernizing clinical data management. Hear their agenda for the future, technology investments priorities, and how partnering with Veeva helps deliver on their vision.

Mayank Anand GSK
VP and Global Head Data Strategy and Management
Leonie Christianson GSK
Business Lead, Vault CDMS Project
Richard Young Veeva
VP, Strategy, Vault CDMS

Labcorp Drug Development modernizes technology solutions to streamline the clinical trial delivery model. Hear Labcorp’s president of clinical operations describe the thorough vetting of Vault CDMS to provide clients greater agility and reduced costs, plus the adoption of Vault Clinical Suite to support the next generations of clinical trials.

Mark Morais Labcorp Drug Development
President Clinical Operations and Commercial Solutions

Learn how Vault CDMS will change, and why, over the next 12 months, from meeting customer requests, to expanding Vault Connections, and launching Veeva CDB.

Drew Garty Veeva
Chief Technology Officer, Vault CDMS
Richard Young Veeva
VP, Strategy, Vault CDMS

Hear how Kronos Bio uses Vault EDC to simplify complex oncology casebooks and to streamline the study build process. Learn three ways they’ve made data entry easier for sites and how automated data flows will reduce duplicate data entry.

Jennifer Neumann Kronos Bio
Director, Clinical Data Management and Programming

Join this fireside chat with Vanderbilt for the site’s perspective on when casebooks should go live, reporting and dashboards they’d like, and what makes a good CRF. Also hear about working with Vault EDC from a performance, training, and user experience.

Alesia Pruitt Vanderbilt Clinical Trials Center
Research Coordinator II
Jill Janssen Vanderbilt University Medical Center
Director

Eli Lilly shares best practices and lessons learned from deploying a library of standards in Vault EDC. Gain advice on building a library with visit structures and cross-form edit checks, CRF tracking and management, and naming conventions for rules.

Jenn Showalter Eli Lilly and Company
Research Scientist – Clinical Study Build
Mita Valera Eli Lilly and Company
Senior Team Lead, Study Build Programming

Learn the latest in this interactive demo and Q&A focused on Vault EDC. Discover how to optimize site, CRA, and data management processes with the latest capabilities in these three purpose-built interfaces.

Michelle Munro Veeva
Solution Consultant, Vault CDMS
Faisal Sufi Veeva
Director of Strategy, CDMS

Complex trial designs pose challenges for study builds. Learn how Vault EDC speeds study builds and eliminates the need for multiple matrices, repetitive forms, or custom programming.

Sharmin Nasrullah Veeva
Manager, Solution Consulting, Vault CDMS

Learn how clinical teams can share enrollment, monitoring, and subject visit information using the Vault CDMS to Clinical Operations Connection. The demo will show how data flows to facilitate trip reports, automate site payments, and manage protocol deviations.

Alice Foltyn Veeva
Solutions Engineer

Learn how sites trigger the creation of dynamic visits and forms precisely when relevant for their subjects. See the rules-based progressive display in action and also how Veeva’s Local Labs module, real-time edit checks, and form linking save time and reduce data entry for sites.

Sharmin Nasrullah Veeva
Manager, Solution Consulting, Vault CDMS

One day to learn from the best in life sciences