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Site Support: The Cornerstone of the Digitalization of Clinical Trials

This event is now available on demand.
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
IQVIA

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.




Kelly Sanford  
Head of Site Operations, Site Enablement Solutions and Decentralized Trials   
IQVIA 

Kelly is IQVIA’s Head of Site Operations, Site Enablement Solutions and Decentralized Trials, part of the Patient Centric Solutions. In her role as Head of Site Operations for IQVIA Decentralized trials, Kelly supports sites and study participants in Decentralized Trial delivery, leading a team of Remote Study Coordinators and Remote Study Assistant team members. Kelly joined IQVIA in 2002 and has served in numerous roles within clinical research as a Study Coordinator, CRA, Clinical Lead, Clinical Project Manager, and management roles. Prior to joining IQVIA DCT, she served in oversight/line management for Clinical Leads. 




Kat Burns       
Project Manager, Research Nursing and Phlebotomy Solutions (RNPS)          
IQVIA  

Kat Burns   is a Project Manager for the Research Nursing and Phlebotomy Solutions (RNPS). Kat oversees the startup process for RNPS projects, focusing on operationalizing the trial assessments and bringing the study to the patient's home as an extension of the investigator site. Kat has over 10 years of clinical research experience, having focused the last 5 years in the home health care space of clinical trials and building this type of service for optimizing Patient Access to Clinical Trials. 
    

For any technical questions please contact Jordan Ramesh: jramesh@mjhlifesciences.com