Clinical Research Coordinator (Onsite) - Trauma Services

Description This position will work at Cox South Hospital, located in Springfield, Missouri. Responsibilities Providing the overall administration and operation of clinical research trials involving the Trauma Service Line. Collecting, maintaining and organizing study information, files, materials and equipment. Scheduling and tracking patient visits. Assisting with regulatory submissions. Performing data entry and managing the timeliness of data submissions. Preparing study materials, e.g., survey and research charts, web‑based materials, etc. Updating and maintaining lists of study subjects. Respondent mailings. Coordinating interview logistics. Maintaining excellent documentation of research decisions and tasks. Performing any additional tasks to support the Trauma Services Department as directed by the Trauma Medical Director and the Trauma Program Manager. Working in a self‑directed team environment while possessing strong organizational skills. Education Required: Bachelor's Degree in a clinical field such as biology, or closely related field. Preferred: Bachelor's Degree in Nursing. Experience Preferred: Previous experience in pre‑clinical or clinical research. Skills Working knowledge of Microsoft Word and Excel. Good written and verbal communication. Strong organizational skills. Ability to multi‑task and prioritize work at given time lines. Licensure/Certification/Registration Preferred: Certified as Clinical Research Coordinator and/or Clinical Research Associate. #J-18808-Ljbffr L.E. Cox Medical Centers