This Clinical Research Assistant I will be responsible for: Under general supervision, coordinating activities of daily operations of clinical research studies. Screening, consenting, recruitment of study participants (e.g. telephone interviews, in-person/remote informational visits), and selection of patients for studies. Screening, consenting, recruitment, and selection of patients for studies. Operating procedures; performing data entry and quality control tasks. Performing other administrative tasks (such as scheduling study visits, completing case report forms, labeling and filing study documents, and maintaining study inventory). Preparing IRB and/or CCI documentation and submissions in conjunction with the Principal Invest