Compile data/collection, and assist in preliminary analysis; maintain research database, assist senior lab members with writing summary reports and report findings to investigator; assist senior lab members in the development of written operating procedures for clinical trial; assist senior lab members with submitting required documentation to IRB. Assist Pl in developing clinical trial protocols; provide clinical enrollment of patients in PI''s research trial; responsible for completing intake for patients and meeting IRB requirements including calling patients and meeting with them to discuss requirements for study and serve as patient resource for concerns and provide information; assist with patient follow-up calls and appointments.