The Clinical Research Assistant I will be responsible for: Under immediate supervision, coordinating the activities of daily operations of clinical research studies. Responsible for the screening, consenting, recruitment, and selection of patients for studies. Preparing IRB and/or CCI documentation and submissions in conjunction with the Principal Investigator and /or other members of the research team. Conducting data collection activities and preparing analytical reports regarding results of studies. Serving as liaison to the families/patients in the research studies, conducted at both on-site and off-site locations, guiding and advising them throughout each phase of the study. Coordinating follow-up visits as necessary. Actin