Sponsors of clinical trials are increasingly overwhelmed by the growing volume of data and the challenges that brings. Moving towards intelligent oversight requires a refocusing of your people efforts on activities that progress your trial. Join Medidata’s Vice President of Product, Trial Management Solutions, Stacey Yount for an insightful discussion about how you can:

  • Work smarter with near real-time visibility into study progress;
  • Identify issues, within a single collaborative environment, before they become problems;
  • Realize better quality and compliance by mitigating risk and optimizing outcomes.

Who should attend: Sponsors and CROs, including Clinical Operations, Project and Program Managers, Finance stakeholders and anyone who manages increasing clinical trial complexity and are interested in ways to more effectively manage clinical trials.

Join this webinar to learn more about how you can move beyond the CTMS data silos and challenges, work smarter with your data, and enable productive collaboration and optimize outcomes.

Featured Speaker

Stacey Yount

Vice President of Product, Trial Management Solutions
Medidata

Stacey Yount has over 19 years in clinical research including experience in clinical data management, clinical operations, statistics, CROs, and central laboratories. Prior to joining Medidata in 2015, Stacey spent 5 years with Covance where she held several leadership positions including Vice President of Project Management, Data Management, and Alliance Management.  Prior to joining Covance, Stacey spent 10 years with Eli Lilly.

Date:  Thursday, August 8, 2019
Time:  1pm ET / 10am PT
Duration:  1 Hour

Register now for this webinar