Making the Most of Trial Data: An Approach to Leveraging Ongoing Study Data for Actionable Insights
On Tuesday, 11th June at 1400 EST | 1900 BST, Marcus Evans Webinars team up with Biorasi to gather a panel of industry experts to discuss talking points surrounding clinic trials data management within the sector;
The average clinical trial now produces over 3 million data points, and that number is increasing rapidly. CROs and sponsors stuck in the old “data management” mentality are finding it increasingly difficult to keep up, let alone move forward.
A smarter approach to clinical data is using advanced analytics and algorithms, combined with early standardization and formatting. This data science approach not only makes data easier to manage, it’s also much more scalable than the traditional approach — perfect for the increasing data requirements of modern and future trials. Best of all, it allows sponsors and CROs to use the data immediately to draw deep insight and provide guidance for individual trials as well as for entire programs.
So why aren’t more sponsors and CROs putting their data to work? Why do so many still treat it as something to be collected and not as a critical tool in clinical development success? In this webinar, Biorasi and Medrio will seek to answer these questions and provide a pathway from data management to data science.
Webinar Agenda Includes:
- Why is clinical trial data increasing, and why will it continue to do so.
- What are some basic requirements for making use of your real-time trial data?
- What tools and techniques are available for sponsors and CROs to work with live trial data?
- How can sponsors use their data to derive real-time insights from live trial data?
- What does the future of data science in clinical trials look like?
Speakers
Director of Product Management
Medrio
As Director of Product Management at Medrio, Becky Capps plays a central role in the development of Medrio’s electronic data capture, eSource, eConsent, and ePRO applications. In her current role, she works on the front line of the advent of eSource in clinical research, helping organizations navigate eSource implementation and regulatory considerations. She brings years of experience in healthcare-focused SaaS to Medrio, with a career that includes senior positions at MatrixCare, SigmaCare, and other companies in the SaaS space. Becky has a Master’s Degree from Georgia State University and is based in Atlanta.
VP, Data Sciences and Biometrics
Biorasi
With over 25 years of clinical trial experience, including a decade as CEO/CTO of a clinical data driven CRO, and a penchant for innovative approaches to clinical study management featuring big data analysis and on-study analytics of live and historical clinical study data, Jon has dedicated his career to developing a systematic and results-focused approach to optimizing the execution of scientific clinical studies. He leverages CDISC Clinical Data Standards (Jon in a CDISC appointed standards trainer), data sciences and artificial intelligence (AI) methods to transform the way that we execute our clinical studies to resolve issues before they create insurmountable problems. He holds an MBA and a degree in Computer Science.
