Clinical data management: The process foundations for a 24-hour study build

22

April

  • 3PM London / 10AM New York
  • Free
  • Why attend?
  • Speakers
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Why attend?

New tools such as AI and machine learning are transforming clinical data management and study builds, but it is imperative that clinical research teams remain in control and stakeholders are aligned throughout.

This webinar will demonstrate how to strike the necessary balance between control and automation, setting the foundations to deliver a 24-hour study build, and taking attendees through the necessary steps to get there.

Experts from Alimentiv (CRO) and Zelta (CDMS provider) will cover protocol interpretation, CDMS pre-configuration, database build, validation, and export – providing both perspectives. The event will demonstrate how the Zelta platform empowers clinical research teams while leveraging new technologies.

Key learnings:

  • How to get from protocol to EDC more efficiently
  • New study build concepts
  • Strategies to leverage AI most effectively in the study build process
  • The advantages of Zelta, a unified cloud-based clinical data management platform

Speakers

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Mark Laney
Sr Director, Sales Engineering & Partnerships, Zelta

Mark Laney has more than 20 years of experience with software in the Life Sciences industry focused on delivering the right solutions for customers. As Sr Director, Sales Engineering & Partnerships, he is tasked with solving customer challenges using the breadth of functionality and flexibility of Zelta’s unified clinical data management solution while facilitating partnerships with complimentary industry leading vendors to offer customers a robust technology solution for their clinical needs.

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Chris Walker
Senior Director, Clinical Data Sciences, Alimentiv

Chris Walker is the Senior Director of Clinical Data Sciences at Alimentiv, where he has cultivated a 12-year career dedicated to advancing clinical research through data-driven solutions. With a strong foundation in Clinical Data Management, his expertise lies in the successful implementation and optimization of eClinical technologies to drive efficiency and insights within the clinical trial process.

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