With the emergence of decentralized clinical trials, we now have a window into patients’ clinical trial experiences like never before. Not only are we collecting more, and arguably better, data through real-world direct patient reporting, but data is also coming from a broader range of sources, including sites, labs, devices, CROs, EHRs, and RWD. This greater access provides us with new, more accurate ways to measure outcomes—and unlocks previously unobtainable insights.

The ultimate goal of using digital and decentralized research methods is to remove burden from the entire clinical continuum. But, while hybrid study designs might, on one hand, make patient participation easier, new pain points have simultaneously been introduced for study administrators and clinicians.

How do we ensure sponsors, sites, and study teams can efficiently and easily manage this wealth of new data to deliver actionable insights? And, how can we streamline complex data sets into a single and actionable source of truth?

Listen in as our experts explore these questions and more, including:

·       How to operationalize decentralized clinical trial study designs.

·       How innovative data capture methods (e.g., sensors and wearables) can improve the quality of patient data.

·       How to solve operational headaches at sites with streamlined workflows to ease reporting and data management.

·       How the magnitude and multi-source nature of data captured in today’s decentralized trials requires systems capable of aggregating and integrating to provide a single source of truth.

·       How innovative trial designs can be offered at scale now to drive operational efficiencies, deliver tomorrow’s powerful insights, and remove burden from the clinical continuum.