It’s Never Too Late: Improve Clinical Trial Processes with a Unified Platform

Clinical Trials, Life Sciences, Pharmaceutical,
  • Thursday, February 28, 2019 | 12pm EST (9am PST)
  • 60 min

As scientific innovation has led to new trial designs, modern cloud technologies have enabled the industry to better manage how clinical trials are executed.

Newer, more advanced cloud applications now offer unified data and process models, allowing organizations to manage their end-to-end clinical trial process within a single system. Rather than juggling individual point solutions, innovative organizations are using a unified clinical platform for greater efficiency, quality and speed of execution.

 Join Veeva and Idorsia to learn how your organization can leverage a unified clinical operating model and drive new levels of efficiency across the entire clinical ecosystem.

 In this webinar, you will:

  • Hear how Idorsia is leveraging state-of-the art technologies to optimize clinical trial processes and accelerate innovation
  • Explore how a unified clinical operating model can simplify and streamline study execution
  • Learn the steps your organization can take to improve visibility, oversight, and collaboration
  • Identify and quantify the value of a unified clinical landscape for your organization

Speakers

Jim Reilly, VP, Vault Clinical, Veeva Systems

As the global head of strategy for Vault Clinical, Jim Reilly is responsible for the overall market strategy and direction of the Veeva Vault Clinical Suite. Jim has over 15 years of experience in the life sciences space in both the clinical and regulatory domains. He started off his career in regulatory eSubmissions as the life sciences space moved from paper to electronic in the early 2000’s. He was then part of a core team at Octagon Research that brought one of the first regulatory publishing and submission management solutions to market. In the latter part of his career, Jim has held a variety of senior software positions, where he was responsible for build, delivery and market strategy for clinical metadata standards systems.

Message Presenter

Simone Mechler, Associate Director, Clinical & Quality Systems, Idorsia Pharmaceuticals Ltd.

Simone holds a degree in biology from the University of Freiburg, Germany. She has over 10 years of consulting experience in pharmaceutical R&D, strategy development, process optimization and restructuring programs as well as system implementations. In 2011, Simone joined Actelion Pharmaceuticals as eClinical Program & Change Manager. She transferred to Idorsia Pharmaceuticals when it was created in June 2017 as part of the acquisition of Actelion by Johnson & Johnson. Simone is responsible for the implementation and support of Idorsia’s Clinical & Quality Systems landscape and is System Owner of Veeva Vault.

Message Presenter

Who Should Attend?

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

  • Trial Master File (TMF) Management
  • Clinical Records Management
  • Clinical Trial Management
  • Clinical Operations
  • Clinical Trials Associates (CTAs) / Clinical Research Associates (CRAs)
  • Site Management
  • Study / Study Start-up (SSU) Management

What You Will Learn

  • Hear how Idorsia is leveraging state-of-the art technologies to optimize clinical trial processes and accelerate innovation
  • Explore how a unified clinical operating model can simplify and streamline study execution
  • Learn the steps your organization can take to improve visibility, oversight, and collaboration
  • Identify and quantify the value of a unified clinical landscape for your organization

Xtalks Partner

Veeva

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 650 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 www.veeva.com.

You Must Login To Register for this Free Webinar

Already have an account? LOGIN HERE. If you don’t have an account you need to create a free account.

Create Account