• ERT and Bioclinica are now Clario. Find out more about our new name, and why we have come together.

Your using an unsupported browser. Please update to a modern browser for a better experience.

Outsourcing in Clinical Trials East Coast

May 24, 2022
May 25, 2022
ET
Valley Forge Casino Resort Event Center, King of Prussia, PA

Discover effective strategies for outsourcing clinical trial operations to ensure trials run smoothly and within budget.

After a two year hiatus, Arena International are delighted to announce Outsourcing in Clinical Trials East Coast will be returning as a physical event in King of Prussia in May 2022!

Join us for a two-day event filled with case studies, panel discussion, and face-to-face networking opportunities around clinical operations, technology and innovation, and data management.

Session Information:

Title: Optimizing ePRO Data in Decentralized Trials

Date: Wednesday, May 25th, 2022

Time: 11:30 a.m. EST

For clinical trials to detect a true treatment effect, the measurement approach must be reliable and valid. With current regulatory guidance to incorporate Patient Reported Outcomes (PROs) as critical endpoints, it is crucial that studies utilize evidence-based decisions in the design, deployment, and management of PRO data. PROs inherently rely on participant buy-in, comprehension, and motivation to contribute to the advancement of medical and scientific knowledge. In this presentation, we will look at:

  • Strengths and limitations of PROs, with specific attention to optimizing these endpoints in decentralized trials that deploy ePRO data capture technology
  • Reducing the time to unlock more accurate clinical evidence needed to bring new treatments to market by incorporating these methods

Speakers

Jessica Emerson Headshot

Jessica Emerson, PhD, MS

Scientific Advisor at Clario

Dr. Emerson is a scientist with over 15 years of experience in behavioral and social science research focusing on the role of technology in measuring and intervening on health behaviors. She has extensive experience in eCOA database design and management. She is currently a Scientific Advisor at Clario, a global data and technology company that helps to minimize risk in clinical trials. In her current role she supports sponsors and CROs in eCOA design best practices and preliminary study set-up to optimize the reliability of eCOA data.