JOB SUMMARY: Position is in the Department of Research. Under limited supervision, position supports the system wide clinical research efforts, coordinates Research Coordinator (RC) program activity, including clinical trial, regulatory affairs and clinical trial and research data coordination. Prepares regulatory documents and monitors regulatory activities for assigned clinical trials. Manages day-to-day regulatory/protocol maintenance operations of the assigned clinical trials. Identifies training and development opportunities for self. Compiles statistical and quality reports on a recurring as needed basis and communicates the findings to the appropriate parties. Maintains high standards for performance for all work related tasks.
REQUIREMENTS: Basic professional knowledge; equivalent to a Bachelor's degree; working knowledge of theory and practice within a specialized field. Biological sciences or related background preferred. Less than 1 year of experience.