Designing an EDC System to Work For a CRA

Clinical Trials, Life Sciences,
  • Thursday, April 25, 2019 | 1pm EDT (10am PDT)
  • 60 min

Targeted source data verification (SDV) might be well established, but many clinical teams are still verifying 100% of their data, making monitoring costly and inefficient.

Join this webinar as established RBM experts share the measures and metrics that organizations need to realize the true value of targeted SDV. Learn better ways to implement a risk-based strategy for SDV to ensure that CRAs focus on the most important data and how doing so can:

  • Improve data quality
  • Speed data collection and analysis
  • Result in higher confidence and user satisfaction

Learn how Veeva is reinventing EDC to work for a CRA, creating significant speed and quality improvements.

Keywords:

Speakers

http://Dawn%20Anderson,%20Deloitte

Dawn Anderson, Managing Director, Life Sciences Strategy and Operations, Deloitte

Dawn has more than 30 years of industry and consulting experience in pharmaceutical, biotechnology, CROs, and technology companies. Her practice is focused on clinical development and she works with clients to design and deploy global operating strategy, performance improvement and technology implementations across the development of new drugs, biologics and devices. Dawn has spoken frequently about clinical transformation and the future of clinical trials, including topics around adaptive design, protocol complexity, risk assessments and the use of technology including virtual trials, digital, mHealth and the use of clinical analytics platforms and cognitive automation in transforming clinical trial delivery.

Message Presenter
http://Drew%20Garty,%20Veeva

Drew Garty, Chief Technology Officer, Veeva Vault CDMS, Veeva

Drew Garty’s career in pharmaceutical technology spans over 20 years and includes significant expertise in EDC, clinical site monitoring, platform integrations and clinical trial management solutions. Drew’s innovative solutions in risk-based monitoring earned him a prestigious industry “Clinical Innovator of the Year” award in 2015. Drew joined Veeva in 2016 as Vice President of Product Management, and led the ground-up design of Veeva’s Vault EDC solution. In his current role of Chief Technology Officer at Vault CDMS, Drew shares and collaborates with customers, partners and the industry to set vision and direction of Veeva’s CDMS product.

Message Presenter

Who Should Attend?

Senior professionals working with clinical data/clinical documentation, including:

  • Clinical Development/ R&D
  • Clinical Data Management
  • eClinical Operations
  • Data Monitoring & Management
  • Development Strategic Operations
  • Information Strategy & Analytics, Clinical Informatics & Innovation
  • Information Technology, R&D IT
  • IT R&D Business Partner

What You Will Learn

How to implement a better risk-based strategy for SDV to:

  • Improve data quality
  • Speed data collection and analysis
  • Result in higher confidence and user satisfaction

Xtalks Partner

Veeva Systems Inc.

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 700 customers, ranging from the world’s largest pharmaceutical companies to emerging biotechs. Veeva is headquartered in the San Francisco Bay Area, with offices throughout North America, Europe, Asia, and Latin America. For more information, visit veeva.com.

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