Site Support: The Cornerstone of the Digitalization of Clinical Trials



Webinar Date/Time: Thursday, October 12th, 2023 at 11am EDT | 8am PDT | 4pm BST | 5pm CEST

Join IQVIA experts as they explore the strategic solutions that help to dissolve the traditional barriers for the site and add accessibility to trial designs that revolutionize workflows and amplify collaborations among sponsors, sites, and patients.

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Event overview

We know that study enrollment, protocol complexity, and staffing pose significant challenges within the industry, especially for clinical research sites. If we continue using conventional approaches of the past, we can’t pave the way for operational success in today's modern trials.

Join IQVIA experts in a thought-provoking webinar that approaches these challenges from the clinical research site perspective. We'll delve into strategic solutions that break down the traditional barriers and add accessibility to trial designs. By doing so, you’ll reduce the burden on sites while increasing the opportunities for the right patients to participate.

Learn how strategic site support and specialty services can revolutionize your workflows and amplify collaborations among sponsors, sites, and patients. Discover the technologies and processes that will transform your partnerships and drive operational success in patient-centric trials.

Three key take-aways

  1. Addressing site obstacles and concerns: Gain insights on how to evolve trials through the digitalization of clinical research while effectively tackling site-specific barriers and concerns related to patient enrollment.
  2. Enhancing trial accessibility and site operations: Uncover methods to implement digital components and models that simplify site operations, improve data quality, and streamline data collection.
  3. Navigating regulatory and legal frameworks: Learn how to establish extended site collaborations that abide by data privacy laws and Good Clinical Practice (GCP) standards to achieve regulatory compliance while maintaining successful partnerships..


Eric Klaver
DCT Regulatory Director

Eric brings 30+ years of clinical research experience to IQVIA in roles varying from data management to post-trial access. His focus has been on compliance in clinical trials, through training and auditing. Eric has trained clinical research staff literally around the world and has audited, supported audits and inspections on an international stage as well. Currently, Eric focuses on the continued compliance of the IQVIA DCT strategy and platform.

Rebecca Sayers, Ph.D.
Director, Patient Centric Solutions

Rebecca is a Director, Patient Centric Solutions at IQVIA. She holds over 12 years of experience within the clinical research industry, specifically in site engagement & enablement. Her experience supporting sites and investigators across multiple therapeutic areas, including oncology/hematology, immunology, neurology, infectious disease helps her team develop and deliver mitigations to site resourcing gaps that affect clinical trial site performance.

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