What is a clinical data monitor?

A Clinical Data Monitor is a professional responsible for overseeing the accuracy, integrity, and security of data collected during clinical trials. They ensure that clinical trial data is collected, entered, and reported according to regulatory standards and study protocols. Their work helps maintain the quality of data used to assess the safety and effectiveness of new drugs or medical devices. Clinical Data Monitors often collaborate with clinical research coordinators, data managers, and regulatory authorities to ensure compliance and resolve any data discrepancies.