Clinical Research Coordinator

Overview The responsibility of the Clinical Research Coordinator I is to assist in providing the overall administration and operation of clinical research trials at CoxHealth. This position requires basic knowledge of clinical protocols and good clinical practices, as set forth by federal regulations and guidelines. Along with the investigators and the research staff, this position is responsible, as determined by the Director of Clinical Research, for assisting with the daily activities of 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 related materials, e.g., survey and research charts, web-based instruments, etc.; updating and maintaining lists of study subjects; respondent mailings; coordinating interview logistics; and maintaining excellent documentation of research decisions and tasks; any additional tasks to support the Clinical Research department and its objectives, as needed. Responsibilities The above description describes the responsibilities of the role, including assisting with the administration and operation of clinical research trials, supporting regulatory submissions, data entry, documentation, scheduling, and study materials. Qualifications Education Required: Bachelor\'s Degree OR current Healthcare Credentials AND 2 years of experience Experience No experience required Skills Strong organization skills; Ability to multi-task and prioritize work to given time lines; Good written and verbal communication; Working knowledge of Microsoft Office software (Word, Excel, PowerPoint, Outlook) Licensure/Certification/Registration N/A #J-18808-Ljbffr