We are seeking an experienced Clinical Research Associate to join our team and participate in all research activities of the Jonsson Comprehensive Cancer Center Clinical Research Unit at UCLA/UCLA Santa Monica and Westwood while under the direction of the team leaders, investigators, Financial Administrative Office, Faculty Director, Medical Director, and Senior Research Director. You will be responsible for completing the data management of clinical research studies and for collection and transcription of research patient data and study related information into research records and assist with maintenance of regulatory files to fulfill research requirements. In this role you will work with study monitors to process and collect accurate data in a timely manner and assist investigators and study coordinators in clinic settings. Work flexible hours and/or overtime to meet study deadlines and requirements. Work may be assigned by the team leader, investigator or Administration, and assignments may be changed on an as-needed basis in order to ensure that studies and patient care needs are handled appropriately and in a timely manner. Salary range: $24.28-$48.04/Hour

Required: * Demonstrated working knowledge of current medical terminology specific to oncology, to accurately read entries in patient charts and record accurately and timely, information into study records and other appropriate research data forms. * Clinical research experience, with in depth knowledge of clinical oncology as it pertains to clinical trials and studies. * Demonstrated knowledge of "good clinical practices" for clinical research as defined by the FDA. * Demonstrated organizational skills to efficiently and effectively provide data management/monitoring support for multiple clinical trials and projects, providing accurate information in a timely manner. * Demonstrated knowledge of all components the research process as it pertains to clinical trials and studies, i.e., IRB procedures and processes, data management, patient care management, etc. * Ability to understand that work may be delegated by more than one person, depending on the individual needs of the clinical study and to carry out job responsibilities as assigned in a timely manner. Notify direct supervisor of any conflicts in demand on time or priorities. * Computer skills using PC platform computers with proficiency in Excel, Word, FileMaker pro to enter data and generate correspondence accurately. * Ability to work at more than one site, travel to participating clinics and attend off-site staff meetings, conferences and investigators meetings. * Ability to work flexible hours to accommodates research procedure and deadlines.