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Wednesday, June 29 • 10:30am - 11:45am
#313: The Future of Clinical Research Data: 2020 and Beyond

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Limited Capacity seats available

Component Type: Forum
Level: Advanced
CE: CME 1.25; IACET 1.25; RN 1.25

This forum will engage a panel of experts who will discuss current and emerging opportunities and trends in the representation and use of research data and describe a future vision for capitalizing on these to improve the future research process.

Learning Objectives

Describe current state, trends and opportunities such as data transparency, electronic health records, interoperability, wearable technologies, regulatory science, data standards and analytics; Describe a vision for future clinical research data systems and processes that can logically evolve from the current state to meet these requirements including opportunities to improve the research process.


Wayne R. Kubick, MBA


Dave Evans, MS

Armando Oliva, MD

Kenneth A. Getz, MBA

avatar for Wayne Kubick

Wayne Kubick

Chief Technology Officer, HL7
Mr. Kubick is CTO for Health Level Seven International, intent on improving clinical research through technology and data standards. He was formerly CTO and a Board member for CDISC, and has 2+ decades in a variety of leadership roles in clinical R&D with BBN, Parexel International (CIO), and a 12 year ride as a senior executive at Lincoln Technologies, Phase Forward, and Oracle Health Sciences. Mr. Kubick holds a B.A. from the University of... Read More →

avatar for Dave Evans

Dave Evans

Managing Director, Accenture
Dave Evans is a senior technology and clinical research executive with over 35 years of experience in the clinical research, regulatory and healthcare industries. He is recognized industry-wide as a leading technology visionary for developing and implementing complex process and system solutions and he now currently serves as Head of Quality Governance and Regulatory Compliance for Accenture R&D Services.
avatar for Kenneth Getz

Kenneth Getz

Director & Associate Professor; Chairman, CISCRP, Center For the Study of Drug Development, Tufts University School of Medicine
Ken is the chairman of CISCRP, and the Director of Sponsored Research / Associate Professor at Tufts CSDD. He is a well-known speaker and author, and serves on a number of for-profit and not-for-profit boards and committees. Ken holds an MBA from the Kellogg School of Management at Northwestern U.
avatar for Armando Oliva

Armando Oliva

President and Chief Medical Officer, Semantica LLC
His expertise includes clinical data standards, regulated study data submissions, and regulatory submission and review policy. A former Associate Director for Informatics in OCS, he focused on developing, adopting, and implementing clinical data standards to support premarketing assessment of new drugs and worked on numerous projects to streamline the receipt, validation, storage, retrieval, and analysis of clinical trial data for regulatory... Read More →

Wednesday June 29, 2016 10:30am - 11:45am
204B Pennsylvania Convention Center 1101 Arch Street, Philadelphia, PA 19107 USA