Clinical Research Coordinator-Endocrinology, Diabetes and Metabolism

Clinical Research Coordinator This role coordinates and performs daily clinical research activities in accordance with approved protocols administered by the non-cancer Clinical Trials Management Organization for the Division of Endocrinology, Diabetes and Metabolism. Key responsibilities include: Assess patient records to identify eligible participants for specified clinical research protocols. Recruit, interview, and enroll patients, obtaining informed consent and ensuring compliance with regulatory and sponsor requirements. Educate patients and families about the purpose, goals, and processes of the study. Coordinate scheduling and follow‑through of patient care appointments, procedures, and diagnostic testing in accordance with the study protocol. Participate in the collection, processing, and evaluation of biological samples. Administer, evaluate, and calculate standardized scoring of diagnostic, psychological, or behavioral testing or questionnaires. Monitor patients for adverse reactions, notify appropriate clinical professionals, and document unfavorable responses for research sponsors and regulatory agencies. Ensure compliance with Institutional Review Boards, FDA, and federal, state, and industry sponsor regulations. Assist with coordinating and preparing for external quality assurance and control reviews. Collect, extract, code, and analyze clinical research data; generate reports to ensure validity of data. Lead coordination of the overall PowerBP+ program, including the Achieving Cardiovascular Excellence, Hypertension Quality Improvement Program, Exercise is Medicine, and Food is Medicine initiatives. Assist with development of new research protocols and contribute to establishing study goals to meet protocol requirements. Minimum Education Required Bachelor's Level Degree or equivalent in biological sciences. Required Qualifications Bachelor's Degree in biological sciences, health sciences, social sciences, or another medical field, or an equivalent combination of education and experience. One year of experience in a clinical research capacity. Knowledge of medical terminology (desired). Clinical research certification from an accredited agency (desired). Computer skills required; experience with Microsoft Office applications (desired). Successful completion of a background check. Qualified candidates may be required to complete a pre‑employment physical, including a drug screen. The university is an equal opportunity employer, including veterans and disability. #J-18808-Ljbffr