Improve Site Experience with Data-Driven Protocol Design



Webinar Date/Time: Wednesday, June 12th, 2024 at 10am EDT | 7am PDT | 3pm BST | 4pm CEST

Do you know what challenges are encountered by sites when operationalizing study protocols? In this webinar, learn how specific protocol design elements impact sites’ perception of burden and how this information can be used to improve site experience.

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Event overview

Sites can encounter a wide range of challenges when operationalizing study protocols, including the need to manage frequent and lengthy patients visits, coordinate complicated procedure schedules and utilize multiple disparate technology systems. Applied analytics enable data-driven protocol design that can help sponsors mitigate these trial challenges.

Data collected from sites can help uncover specific protocol elements that drive sites’ perception of burden. These findings can be used to optimize protocol design to decrease burden and improve site experience, potentially leading to positive outcomes such as facilitating the collection of cleaner data and improving protocol compliance.

Three key take-aways

  • Uncover key challenges sites encounter when operationalizing study protocols
  • Learn how specific protocol design elements impact sites’ perception of burden
  • See how site burden analytics can be used to improve protocol design


Betsy Wagner
Design Analytics Director

Betsy Wagner has a strong background in clinical site operations, specialized in oncology trials. Her site experience includes both academic centers and community-based sites, while working at CROs and recruitment technology service providers. Betsy has built and expanded programs, conducting both NCI and industry sponsored trials, providing a strong foundation in regulatory, feasibility and enrollment operations as well as strategic program growth. While holding these roles, Betsy gained a reputation for success in pressure testing protocols, including consulting with several national groups on smarter protocol design. She recently joined IQVIA, where she leverages her experience to improve clinical trial design for all stakeholders—sponsors, sites, and patients.

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