Webinar: Accelerate Clinical Trials by Simplifying Data Quality

Sponsored by: Informatica

Focused on:

  • Clinical Trials Data Management
  • Compliance

Date: 7 June

474

Time: 1PM New York/6PM London

There is no challenge more critical or costly in life sciences R&D than effectively managing the subject and operational data used in the development of new medical approaches. Poor data quality impacts the overall design, execution, quality, and management of clinical trials.

"The drug development process is predicated upon the availability of high quality data with which to collaborate and make informed decisions during the evolution of a product or treatment." - Informatica customer and CIO of leading Contract Research Organisation.

Simplifying the complexity of clinical trials data management requires certain procedural steps that lead to reduced costs, shorter time to market, increased veracity of results, and improved compliance with industry standards and regulations.

Join John Jones, IT strategist focused on life sciences, and Informatica, the industry leader in all things data, for a webinar showcasing industry best practices that lower the direct cost of poor data management in clinical research studies.

You'll learn more about the strategic data management capabilities needed to positively affect clinical trial cost and duration.

Presented by

John Jones,

IT Strategist focused on life sciences

John Jones is an experienced IT Strategist focused on developing innovative technology solutions for unmet business needs in Life Sciences. Recently John led Quintiles’ IT Consulting Division from 2010 – 2015 focusing on IT Advisory and Implementation services in Life Sciences. John has more than 20 years experience in developing and delivering IT Solutions for various companies, and has extensive experience in the clinical, regulatory, and commercial areas.

His technical specialties include: enterprise architecture planning and definition, long-term technology strategy development, knowledge and content management, information architecture and metadata definition, structured content authoring and data integration/business intelligence platform implementation.

John earned his BS and MBA from Rutgers University in New Jersey.

Bryan Balding,

Senior MDM Solution Specialist

Bryan has been a technical sales specialist for enterprise software solutions for the last 19 years. He has specialized the last 10 years in Master Data Management and Data Quality solutions. He has been a MDM/DQ solution specialist with Informatica since 2012 covering Pharma and Life Sciences.

A graduate of the United States Military Academy, Bryan has a Bachelor of Science degree with a minor in Computer Science.

Monica McDonnell,

Director of Industry Consulting Europe

Monica McDonnell is the Director of Industry Consulting Europe for Informatica. Monica has 15+ years of enterprise software experience, advising global companies on how to gain business insight, optimizing their operations and driving innovation from data.

Her current activities are focused around identifying and quantifying the value well-managed and high quality data can deliver across multiple business processes. Monica earned a B.Sc in Industrial Engineering from the University of Witwatersrand, and a M.Sc in Software Engineering from Oxford University. Both degrees were awarded with distinction.

Key Learning Objectives

  • How to automate the application of CDISC standards
  • Obtaining quality and timely data to support risk based monitoring (RBM)
  • Preparing for the future of alternate data sources, for example from devices, wearable technology, and patient forums

Audience

  • Clinical Trial Operations
  • Bio Statisticians
  • IT
  • Enterprise Architecture
  • R&D
  • Project Managers
  • Senior Managers
  • Directors
  • VP