Summary from listing
The Clinical Research Coordinator manages day-to-day activities for clinical trials, including participant screening, enrollment, monitoring, data collection, study-visit scheduling, adverse-event assessment, and reporting to the sponsor, IRB, FDA, and Data Safety Review Committee. The role may supervise other research staff and coordinates with specialty, clinic, and hospital personnel to ensure protocol and Good Clinical Practice compliance. A bachelor's degree in a related field or four years of related experience, plus two years of relevant experience, is required; oncology research experience and Spanish-speaking ability are preferred. The position is not eligible for visa sponsorship.
