The clinical data team at Vertex asked themselves, how can we reduce our development timelines and costs—make things go faster, for less? 

Answering those questions set Vertex on a path to challenge themselves and their vendors to improve speed without sacrificing quality. As a result, they’re reducing database build times by as much as 50% and reliably lock data in 15-18 days.

This webinar is intended for clinical data executives, heads of clinical, and heads of clinical research.

Attendees will hear:

  • How Vertex reaches 80-90% compliance with sites entering data within 2 days of the event

  • Their #1 goal for transforming the UAT process

  • Their novel recommendation for when to go live

  • The technology strategy supporting their process improvements

Featured Speakers

Vikas Gulati

Senior Director of Clinical Data Management and Metrics
Vertex Pharmaceuticals

Vikas Gulati has over 20 years’ experience focused on clinical data management, data standards and governance. He has led several global cross-functional teams to successful outcomes in Biotech/Pharma and CROs. He is currently the Global Head of Clinical Data Management at Vertex Pharmaceuticals, Inc.   

Richard Young

Vice President, Vault EDC
Veeva Systems

Richard Young has nearly 25 years of expertise in data management, clinical solutions, and advanced clinical strategies. At Veeva, Young is establishing Vault EDC as the leading solution for clinical data management.

Michelle Harrison

Associate Director of Clinical Data Management and Metrics

Michelle Harrison is currently working at Vertex Pharmaceutical in Boston Massachusetts as an Associate Director of Data Management. Prior to joining Vertex, she worked as a consultant for BioBridges. For 2 years there she consulted for a number of small Biotechs assisting with Vendor oversight and start up activities.


Register now for this webinar