Effective portfolio and trial oversight is essential to ensure that all studies are managed consistently, are of high quality and are kept on track. Recent global events coupled with the general industry shift to a risk-based quality management approach for clinical trials have demanded a new outlook on trial management. Moving from a clinical monitor focus to a truly data-driven approach is essential to ensure that data quality is consistently high – even when unexpected restrictions and abrupt changes arise during a trial.
Each part of a study team holds a different piece of the trial management puzzle. Modern trial oversight must bring together all perspectives and pieces in a clinical trial, must be flexible and agile, and must be comparable so the trial can be assessed from both vertical and horizontal views. In this webinar, the presenters will discuss these and additional principles which provide leaders and study team members with visibility and control and enable proactive, informed decision-making.
Register for this webinar to hear insights into clinical trial management from the experts at Covance by Labcorp.
Kristin Stallcup, MS, PMP, Senior Director, Xcellerate Customer Success, Covance by Labcorp
Kristin Stallcup brings 15 years of industry experience in various trial management capacities. Currently, she serves as senior director responsible for implementation and adoption of the Xcellerate technology suite into business process. Previously, she served in central monitoring as business lead for the development and implementation of Xcellerate Risk and Issue Management and was also responsible for providing clients with Covance Xcellerate Monitoring methodology and technology implementation.
Kristin has held other industry positions ranging from clinical research associate to project director. Kristin received her MSHS in clinical research management from George Washington University, her BS in molecular biology from Vanderbilt University, and has Project Management Professional (PMP) certification.Message Presenter
Daniel Kowalski, Senior Manager, Informatics, Covance by Labcorp
Daniel Kowalski has 13 years of professional experience within the industry in the biometrics area, from SAS programming through biostatistics and data management to informatics. Currently, he leads the team responsible for the setup of Xcellerate tools, focuses on expanding the use of Xcellerate and co-leads several enhancements projects. In his previous role, Daniel was responsible for the development and implementation of Xcellerate Data Review.
Daniel received his MSc degree in the field of pure mathematics from Jagiellonian University in Cracow, Poland.Message Presenter
Who Should Attend?
- C-Level Executives in Clinical Trials Management
- Clinical Development Directors/Managers
- Clinical Operations
- Clinical Risk Managers
- Information System Management
- Information Technology
- Medical/Operational Directors
- Project Management
What You Will Learn
Join this webinar to learn about:
- Why shifting from a clinical monitor focus to a data-driven approach is essential to maintain data quality
- How a risk-based quality management approach can help trials weather unexpected restrictions
- The key attributes of modern trial oversight
Covance by Labcorp
Covance by Labcorp is a leading global life sciences company, which provides contract research services to the drug, medical device and diagnostics, crop protection and chemical industries. Employing over 26,000 people worldwide, we provide comprehensive drug development solutions and are on a mission to advance health and power clear, confident decisions.
Covance by Labcorp is a global leader in nonclinical safety assessment, clinical trial testing and clinical trial management services. Our unique perspectives are based on decades of scientific, medical, and regulatory expertise.
Together with our clients, Covance by Labcorp supports the development of innovative, life-changing treatments. Visit us at www.covance.com.