Clinical Research Coordinator - Full-Time

Role Overview Coordinate non-therapeutic clinical research protocols under supervision, ensuring compliance with regulatory standards. Assist with complex studies, participant screening, enrollment, and monitoring. Recognize and report adverse events or protocol deviations. Collect, abstract, and input research data, and perform administrative and regulatory duties related to studies. Key Responsibilities Manage protocol documents, amendments, and study logistics to meet institutional and federal standards.Handle IRB submissions and communicate with study sites and federal agencies.Support protocol development and execution of related tasks as assigned. Qualifications & Skills HS Diploma with ≥3 years experience or Associate's degree with ≥1 year experience; clinical setting experience preferred.Experience in clinical research or related fields is desirable; completion of a study coordinator training program is a plus.Knowledge of medical terminology preferred.No licensure required. Additional Details Nonexempt, full-time position with hourly pay between $24.55 and $35.65.Hybrid role requiring residence within 100 miles of Rochester, MN, with onsite visits twice monthly.Monday to Friday, business hours; no weekend schedule.