According to the 2017 Tufts eClinical Landscape Study, 97% of companies plan to increase use of at least one clinical data source over the next three years. But today, 98% of companies report challenges with their clinical data management systems.
How can companies become more efficient, all the while planning to manage even more data from a variety of sources?
Join Dawn Anderson, managing director, life sciences strategy and operations at Deloitte and Richard Young, vice president of Vault EDC at Veeva as they share how companies are interpreting the research findings and applying them to improve business processes. Learn strategies your teams can leverage to speed study timelines and prepare for increasing amounts of real-world evidence and unstructured data.
After the presentation, 15 minutes will be reserved for an interactive Q&A – register now!
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Dawn Anderson, Managing Director, Life Sciences Strategy and Operations, R&D Practice, Deloitte
Dawn has more than 30 years of industry and consulting experience in pharmaceutical, biotechnology, CROs, and technology companies. Over the past 10 years, Dawn has led strategy and operations solutions across clinical development for clients, focused on innovative clinical productivity, operating model optimization, clinical transformation, organizational redesign, process re-engineering, vendor performance management, and enterprise clinical platform solutions.
Her specialty areas include: clinical transformation and the future of clinical trials, such as adaptive design, the use of digital in clinical trials, risk assessments, patient & site-centricity, and the use of social, mobile, clinical analytics and cognitive automation in transforming clinical trial delivery.
Prior to joining Deloitte, Dawn held executive clinical leadership positions at global pharmaceutical, biotechnology, CROs and technology companies.Message Presenter
Richard Young, Vice President, Veeva Vault EDC, Veeva Systems
As vice president for Veeva Vault EDC, Richard Young is responsible for establishing Veeva Vault EDC as the best in class solution for all data acquisition, management and reporting purposes. With almost 25 years of experience in life sciences, Richard is known for his executive vision and proven operational experience in data management, eClinical solutions, and advanced clinical strategies.
Most recently, Richard served as vice president of global consulting partners at Medidata Solutions, spending spent considerable time consulting on adaptive trials, risk-based monitoring, big data, mobile health, and other major data strategies with sponsors and partner organizations across the globe.
Richard also held operational roles in both pharmaceutical and contract research organizations, such as GlaxoWellcome, Novo Nordisk, Chiltern and PAREXEL, before moving into business development with Cmed.
Who Should Attend?
- Head of Clinical Development/R&D
- Head of Biometrics
- Chief Medical Officer
- VP of Clinical Ops
- VP/Director, Data Management
- Associate Director, Clinical Data Management
- Associate Director, eClinical Operations
- Executive Director, Head of Global Data Strategies and Solutions
- Development Strategic Operations
- Sr Director, Data Monitoring & Management
- Sr Director, Information Strategy & Analytics, Clinical Informatics & Innovation
- Vice President, R&D IT
- Senior Director Information Technology, R&D IT
- Global IT R&D Business Partner
What You Will Learn
- Managing data from a variety of sources
- Preparing for studies that rely on real-world evidence
- Handling increasing amounts of unstructured data
Veeva Systems Inc. is a leader in cloud-based software for the global life sciences industry. Committed to innovation, product excellence, and customer success, Veeva has more than 600 customers, ranging from the world’s largest pharmaceutical companies to emerging biotechs.
Built on a modern unified clinical platform, Veeva Vault EDC allows you to run the trial you want, not the trial your technology limits you to. Quickly deploy studies in weeks and not months, and make in-flight amendments without migrations or downtime. The ability to integrate and maintain complete and concurrent data, including non-CRF data, in a trial provides real-time insight and dramatically improves productivity.