Oncology Trial Complexity: New Tufts CSDD Research and Strategies to Optimize Study Design

Life Sciences, Clinical Trials, Drug Discovery & Development,
  • Tuesday, August 24, 2021

New research from the Tufts Center for the Study of Drug Development provides insights into the unique challenges associated with executing oncology clinical trials: complex scientific and operating design characteristics, more internal reviews, significantly longer cycle times, poorer recruitment and retention rates, and higher numbers of protocol deviations and unplanned protocol amendments. Clinical teams need new strategies and solutions to address these unique challenges and optimize trial performance.

Register for this webinar to hear Ken Getz, director of Tufts CSDD and Richard Young, vice president of strategy, Vault CDMS at Veeva, as they discuss the results of this new research and its implications. See how your trial metrics compare to your oncology peers as Ken Getz shares new benchmark data, including endpoints and procedures, cycle times, screen failure and drop out rates, and the frequency of protocol amendments. Richard Young will outline what you should look for in an EDC so that you can:

  • Build complex studies without risky custom functions
  • Implement protocol amendments quickly and easily
  • Accommodate platform, bucket, umbrella and adaptive trials

Come prepared with questions for our speakers to ask during the dedicated time for Q&A.

Speakers

http://Kenneth%20A.%20Getz,%20Tufts%20Center%20for%20the%20Study%20of%20Drug%20Development%20(CSDD)

Kenneth A. Getz, MBA, Deputy Director & Research Professor, Tufts Center for the Study of Drug Development (CSDD)

Mr. Getz is an internationally recognized expert on R&D and clinical trial management practices and trends, the global investigative site landscape, site management and patient recruitment and retention practices, and the worldwide market for outsourcing clinical research functions. Mr. Getz’s research studies on protocol design complexity and clinical research efficiency and effectiveness, conducted over the past two decades, are considered by many in the research-based life sciences industry to be pioneering work. His 20+ years of original research benchmarking R&D management practices, global outsourcing and the investigative site landscape have contributed to an industry-wide understanding of these critical markets and to improvements in management strategy and execution.

Message Presenter
http://Richard%20Young,%20Veeva%20Systems

Richard Young, VP, Strategy, Vault CDMS, Veeva Systems

Richard Young is VP, Strategy, Vault CDMS at Veeva Systems. Young has over 25 years of expertise in data management and clinical strategy. His broad experience includes roles at Medidata where he focused on adaptive trials, risk-based monitoring, mobile health, and big data. He has also held operational roles at leading pharma and CRO organizations, including GlaxoWellcome, Novo Nordisk, and PAREXEL. Young holds a Bachelor of Science degree in biochemical sciences from Coventry University.

Message Presenter

Who Should Attend?

  • Data Managers
  • EDC Programmers
  • Clinical Operations
  • Clinical Systems Managers

What You Will Learn

In this webinar, participants will learn:

  • Unique challenges and solutions for teams running oncology studies
  • How to accommodate unplanned changes quickly and easily
  • How to consider trial design and technology to optimize trial performance

Xtalks Partner

Veeva

Veeva’s industry cloud solutions provide data, software, services, and an extensive ecosystem of partners to support your most critical functions from R&D through commercial. Veeva Vault Clinical Data Management Suite offers EDC, data cleaning, coding, and review in a single unified suite. You can manage study build through execution and gain a complete and concurrent view of all clinical data within a trial. Vault CDMS accelerates study timelines by reinventing traditional data management systems and processes. Learn more at veeva.com/cdms

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