This Division of Pharmacology is seeking a motivated Clinical Research Coordinator to coordinate investigator-initiated and industry-sponsored clinical trials of targeted theranostic in patients with various types of cancer according to Good Clinical Practices (GCP), internal standard operating procedure (SOPs), and University policies and procedures such as HIPAA guidelines. In this role you will collect and maintain patient data in appropriate digital formats; schedule patients for search visits and procedures, and enroll/disenroll patients on OnCore. You will also assist in screening patients for eligibility using protocol specific inclusion/exclusion criteria, and maintain documentation for each patient. You will also assist with analyzing imaging data; assist in monitoring potential treatment side effects; Assist the PI in development of materials necessary to appropriately document the research. Finally, you will conduct sponsored research studies that require management and interpretation in addition to preparing documentations for patient’s appointment.
UCLA is an Equal Opportunity/Affirmative Action employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or protected Veteran status.