Responsible for performing diversified duties in coordinating all activities related to clinical trials including the screening and evaluation of prospective trial patients, clinical follow-up of enrolled trial patients, correspondence and coordination with the institutional review board and trial sponsors, and management/tracking of compliance with federal and Institution guidelines relating to conducting human subject research while educating patients to clinical trials and obtain informed consent to participate by performing the following duties. Experience Preferred 2 year(s): Clinical Research Education Preferred Bachelors or better Equal Opportunity Employer This employer is required to notify all applicants of their rights pursuant to federal employment laws. For further information, please review the Know Your Rights (https://www.eeoc.gov/poster) notice from the Department of Labor.