The Department of Medicine is looking for a motivated Study Coordinator (Staff Research Associate I) to recruit and survey patients, transplant patients, and/or living donor kidney transplant patients. You will manage patient participants in randomized control trials and epidemiological studies, as well as, organize and prepare educational materials for distribution to study participants. In this role, you will also organize and monitor daily research activities in accordance with the study protocols, keep accurate electronic records and documentation through spreadsheet, database, assist in meeting university regulations for human subjects research (IRB), attend regular staff meetings and associated trainings, conduct quality assurance activities for assigned studies at the site, and manage subject remuneration. Target hourly rate: $24.88-$29.67

Required: * Experience working with survey data using REDCap, Microsoft Excel, and SPSS * Interpersonal and communication skills to effectively relate to patients, their families, members of the health care team, and the lay and professional community. * Good work ethics, strong communication skills, honest, and ability to work well with minimum supervision or as a part of a group. * Organizational skills to track and create patient treatment plans, data collection procedures and the conduct of complex research activities. * Ability to work independently, set goals and objectives, prioritize work activities, and report to the supervisor on a regular basis and in a timely manner. * Ability to manage competing demands/assignments/deadlines. * Willingness to work occasional evenings and weekends * Skills in maintaining research records and completing data/case report forms. * Knowledge of concepts and specific requirements of clinical research. * Knowledge of requirements of Human Subject Protection Committee, i.e., applications and preparation of informed consent forms. Ability to process research protocol approvals expeditiously. Preferred: * BS/BA