ProSciento’s Clinical Monitoring team consists of CRA professionals with focused expertise in metabolic clinical studies. This model is different in the industry, in that our CRAs are not working across several therapeutic areas at once, thus promoting efficiency and focus. Our CRAs are critical to our overall clinical trial management team and implement effective monitoring and risk mitigation strategies, ensuring patient safety, data integrity, and risk assessment. For each study, the lead CRA is the primary point of contact—a best practice that eliminates confusion that sites sometimes face in wondering whom to contact. Moreover, ProSciento’s proprietary CRA Score Card system tracks key performance indicators, including turnaround time for onsite monitoring reports, percentage of SDV backlog, and resolution of Issues in Action, helping to drive site performance and providing real-time actionable reporting.