Nemours is seeking a Causal Clinical Research Assistant. Responsibilities The Clinical Research Coordinator II works under limited supervision, assists with running clinical trials, completes regulatory documentation and tracks Nemours IRB submission and approvals. May assist in the enrollment of human subjects. May provide clerical and technical support to ensure adherence to research protocols and quality of information received. Performs a variety of research and data base collection and processing, as well as clerical duties in support of clinical trials to assist investigators in organizing, gathering and compiling clinical research data.