Data Coordinator II

Monitors data collection and its adherence to protocols. Responsible for the collection, coordination, processing, and quality control of clinical trial data. This is a part time opportunity expect to support 20 hours per week. This role will have the opportunity to work partially at our campus and remotely. Review and edit research protocols with regard to data collection. Review and monitor patient/participant clinical trial data. Abstract and code information such as patient/participant treatment and progress. Perform routine audits to insure quality and completeness of the data submitted. Serve as a liaison and reference resource to Physicians, Investigators, other staff members, and other organizations with questions about data collection or protocol procedures and requirements. Monitor adherence to protocol, investigating any violation. Maintain computer database. Participate in committees with regard to data quality assurance. Maintain ongoing contact with data suppliers to insure timely and complete delivery of data. Assist in the development of data acquisition forms. Work with Biostatisticians and computer application specialists in developing systems for processing data. Assist in the planning and content of statistical reports. Coordinate special projects. Provide input to support policies and goals of the department. Perform other duties as assigned.