Clinical Research Coordinator
CurrentCommunicate directly with pharmaceutical representatives to assess feasibility of clinical trials at the site.Work with a small team or independently to implement new clinical trials at the site or close old studies down.Responsible for management of data for clinical oncology research trials.Work with central and local IRBs to provide regulatory documentation as well as account for patient adverse events.Screen prospective participants in EMR systems for research trials based on study criteria.Ensure patients adhere to study protocol while on study. Organize study files and documentation.Collect and manage patient and laboratory data.Ensure the safety of the trial and materials.Maintain ethical standards and regulations.Track patient health and progress.