How Alcon Enabled Data Managers to Build Studies Directly from the Protocol

Life Sciences, Clinical Trials,
  • Tuesday, July 28, 2020

After spinning out as an independent company, Alcon needed to establish all new clinical systems. As part of building up their data management function, they adopted Veeva Vault EDC and trained their team on the Agile Design build process. Just three months later, Alcon had completed three study builds.

Their data managers are building studies independently by configuring casebooks directly from the protocol, including most validation checks and rules. The clinical programmers cover more advanced checks and rules and use their newly freed time to manage Alcon’s clinical systems and metrics to improve the team’s operating efficiency.

Speaker

http://Leianne%20Ebert,%20Alcon

Leianne Ebert, Head of Data Management, Alcon

Leianne Ebert is the Head of Data Management at Alcon and Business Lead for the implementation of Veeva Vault CDMS. She is an established leader in clinical research with 15 years of experience leading global teams in Operations, Data Management, Standards and Systems.

Message Presenter

Who Should Attend?

  • Data managers
  • Clinical operations
  • Clinical systems managers

What You Will Learn

  • Best practices for adopting a new EDC and enabling your team to build their own studies
  • Data management’s perspective on configuring studies directly from a protocol
  • Clinical programmer’s perspective on using a rules engine and dynamics instead of custom code

Xtalks Partner

Veeva Systems Inc

Veeva Systems Inc. is a leader in cloud-based software for the global life sciences industry. Committed to innovation, product excellence, and customer success, Veeva has more than 700 customers, ranging from the world’s largest pharmaceutical companies to emerging biotechs. Veeva is headquartered in the San Francisco Bay Area, with offices throughout North America, Europe, Asia, and Latin America. For more information, visit veeva.com.

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