Clinical Research Professional I

Coords selected aspects of clinical research studies; recruits and screens patients for enrollment; obtains consent; prepares flowcharts, study-specific source documents, and collects/records data on case report forms; creates databases and performs date entry; maintains participant confidentiality; promotes knowledge of current professional practice and research standards; facilitates collaboration across departments; coordinates/collects data for sponsor review during site visits; assists study monitors in chart and case report form review; maintains files per regulatory standards; performs other duties as assigned; preferred bilingual (Spanish/English).