Clinical Medical Monitoring

Medical monitors play a pivotal role in clinical trials, with their primary focus on ensuring the ongoing safety of trial participants. In addition to this critical responsibility, they are frequently engaged in various tasks such as protocol training, classifying deviations, conducting clinical feasibility reviews, and overseeing study-level safety surveillance, among other duties.

Despite the significant importance and scope of a Medical Monitor's role, their primary tools for review often consist of lengthy listings, manual trackers, and perhaps a few custom reports that required months of programming and still lack utility. Moreover, they frequently find themselves navigating multiple systems to monitor alerts and communicate necessary actions across the team. This cumulatively results in prolonged review cycles, an increased risk of errors, and clinicians feeling overburdened by their workload.

Learn how ThoughtSphere’s ClinReview module optimizes clinicians' time and expertise by automating processes and creating an integrated environment to foster a holistic medical review approach.