Join us in Recognizing Heart Month!
Cardiovascular outcome trials (CVOTs) continue to be an expensive and complex aspect of drug development with numerous challenges including:
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Delivering complex trial design
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Managing stakeholder diversity
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Ensuring patient enrollment & retention
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Implementing innovative technology
On February 28th at 11am ET, Worldwide hosted a case-study webinar, "Tales from the Trenches: The Unique Challenges of Cardiovascular Outcome Trials.”
During this free Heart Month webinar, Worldwide's cardiometabolic leads shared the uncommon approach Worldwide’s medical, scientific and operational experts have taken to ensure a large CVOT, involving more than 10,000 patients across nearly 500 sites in 8 countries, stays the course.
View the recording today!
Karen joined Worldwide in 1993 and is responsible for Global Project Management within the Cardiovascular and Late Phase division. She has more than 22 years of experience in the CRO industry and has worked on numerous large cardiovascular outcome studies conducted by the group, including INJECT, GUSTO III, InTIME-II-TIMI 17, OPUS-TIMI 16, PROVE IT–TIMI 22, CLARITY–TIMI 28, MERLIN-TIMI 36, where she held the position of Global Project Manager/Director . In 2003, Karen took over as head of the Project Management department, which included the management and supervision of the company’s project managers, CRAs and the IVRS development and support teams. Karen currently heads the Global Cardiovascular Project Management division at Worldwide Clinical Trials and continues to supervise a global team working on both large cardiovascular outcome studies, as well as other phase II-IV studies in other cardiovascular indications.
Nancy Newark joined Worldwide in July 2010 and has provided operational oversight and leadership for numerous cardiovascular projects. She currently serves as a franchise lead within the cardiometabolic therapeutic area. Prior to joining Worldwide, Ms. Newark worked at Duke University Medical Center for 25 years. For 11 of those years, she was a critical care transport nurse for the helicopter and ground ambulance program, and for 14 years, she provided senior operational leadership for global multi-center clinical trials and registries, including direct responsibility for regulatory compliance, strategic development of project management, site management, and clinical monitoring services at the Duke Clinical Research Institute (DCRI).
Christie has worked in clinical research for more than 13 years and has worked for Worldwide Clinical Trials since November of 2016. She began her career in research in Data Management as a nurse-reviewer of clinical data. Christie then worked as a Lead Data Manager for several years, before taking her experience into the technical arena. While working for an EDC provider, Christie was able to gain experience in how databases are built from the ground up, and work with individual clients around the world. She then returned to Data Management as a lead, overseeing all activities from kickoff meeting through Database Lock. Christie has worked across various therapeutic areas, specifically Cardiology and Oncology on Phase I through IV studies.
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About Worldwide Clinical Trials
Worldwide Clinical Trials employs more than 1,600 professionals around the world, with offices in North and South America, Eastern and Western Europe, Russia and Asia. Founded by physicians committed to advancing medical science, Worldwide is out to change how the world experiences CROs – in the best possible way. From Early Phase and Bioanalytical Sciences through Late Phase and post approval, we provide world-class, full-service drug development services. With infrastructure and talent spanning 60 countries, we execute predictable, successful studies with operational excellence. We never compromise on science or safety. We’re never satisfied with the status quo. We’re the Cure for the Common CRO. For more information, visit Worldwide.com.