Sarah Cannon September 2018-PresentSenior Research Nurse Supports enrolling patients onto clinical trials through recruitment, screening, enrollment and follow up of eligible subjects according to protocol requirements. Ensures the protection of study patients by timely adherence to protocolrequirements/compliance Adheres to appropriate Standard Operating Procedures Is familiar with the protocols on which the patients are enrolled Uses the protocol as the only tool to screen, treat, and follow patients Reviews the study design and inclusion/exclusion criteria with physician and patient. Complete and document screening/eligibility accurately Complete and document the informed consent process accurately and have all parties fullyexecute the document including HIPAA Authorization Complete the inclusion/exclusion form and standard enrollment form accurately Document all specific tools required by the protocol (i.e. oral medication forms, pill countdiaries, quality of life questionnaires, neuro exams, vital signs sheets, times of PK draws, etc.) Screen every new patient or patient returning to office with scan results and documentappropriately on the patient tracking logs Ensure that all medications, including antiemetics, are approved by the registrar prior toinitiating treatment or when changing medication regimens, such as crossover studies Accurately calculate and document the BSA, creatinine clearance, urine protein: creatinine ratioor any other conversions needed per protocol Document any interaction regarding the patient that occurs while the patient is enrolled on aprotocol, including follow-up and survival (this includes home health intervention, pharmacies,study managers, physicians, and clinic colleagues) Ensure that follow-up appointments, scans, or any related procedures are scheduled correctlyaccording to protocol requirements Accurately complete all data and query requests and submit with source documentation withinthe timeframe specified by the study manager. Obtain completed and signed waivers prior to submitting forms to enrollment coordinator forinvestigator-initiated protocols Reconsent patients in a timely manner and document process appropriately Accurately completes initial SAE report and submits to the Safety Department within 24 hours ofbecoming aware of the event Accurately completes and submits follow-up SAE report to the Safety Department within thetimeframe allotted by the Regulatory Department.