Tufts Research: Strategies from Data Management Leaders to Speed Clinical Trials

Learn how top pharmas and CROs plan to speed database build and data collection, as well as their top challenges and future priorities.

Join this webinar to gain insights into:

• Taking an agile approach to database build
• Reducing user acceptance testing (UAT) timelines with a risk-based approach
• Driving innovation at your organization

This in-depth research from Tufts follows their industry-wide eClinical Landscape Study, examining the major cause of database build delays and their impact on trial cycle times.

Speakers

Ken Getz, Director of Sponsored Programs, Tufts CSDD

Ken Getz is an internationally recognized expert on pharmaceutical R&D management, protocol design, outsourcing, data management, investigative site management and patient engagement. Mr. Getz has published extensively in peer-reviewed journals, books, and in the trade press. Ken is also the founder of CenterWatch, a leading publisher in the clinical trials industry.

Message Presenter

Richard Young, Vice President, Vault CDMS, Veeva Systems

With almost 25 years of experience in life sciences, Richard is known for his executive vision and proven operational experience in data management, eClinical solutions, and advanced clinical strategies. Most recently, Richard served as vice president of global consulting partners at Medidata Solutions, consulting on adaptive trials, risk based monitoring, big data, mobile health, and other major data strategies with sponsors and partner organizations across the globe.

Message Presenter