This role shall also be responsible to serve as the liaison between the clinical trials staff and the departments conducting clinical trials by screening, identifying, and referring patients for enrollment by the Research Nurses; taking on-call responsibility during off-hours such as nights and weekends; collecting and maintaining pertinent CVs, Medical Licenses, CITI Training, and FCOI Disclosures and training certifications; and completion of both internal and external feasibility questionnaires. This will include, but is not limited to: (a) medical record review for pre-screening of eligible patients, (b) completion of feasibility questionnaires and obtaining signatures as necessary, (c) CRF completion and data entry, (d) research chart prep for audits, (e) maintaining regulatory files such as CVs and Medical Licenses, CITI training, and FCOI Disclosures, (f) identify new clinical trials and review for enrollment feasibility, and (g) provide on-call Clinical Trials coverage as needed.