The award-winning MedSource CRA team is one of the finest clinical monitoring teams in the industry, ensuring protocol and regulatory compliance, and timely submission of high-quality data. Educational backgrounds range from registered nurses to MDs, bringing vast therapeutic background and experience. Each monitor is experienced and trained in FDA regulations, ICH guidelines, and GCP compliance.
Because Clinical Monitoring is the backbone of our business model, we can state with confidence:
- Our expertise means query rates consistently lower than the industry average. This excellence gives greater accessibility to key information needed in making timely drug development decisions.
- Our clinical research associates average more than 10 years of monitoring experience, with the majority in oncology, CNS, and infectious diseases.
- Our monitors can directly participate in data management processes, promoting closer integration between data management and site activities, resulting in higher-quality clinical data throughout the entire process.
- Because our monitors work within their chosen therapeutic areas, we retain an established group of experienced monitors who develop long-standing relationships with our investigators and sites.