ResponsibilitiesParticipate in all research activities as part of the clinical research team located at team located 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 of the JCCC CRU.
The Clinical Research Associate is responsible for completing in a timely and accurate manner the data management of clinical research studies.
Responsible for collection and transcription of research patient data and study related information into research records assist with maintenance of regulatory files to fulfill research requirements.
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.Qualifications 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.
Experienced in performing assessments and interventions under the direction of the principal investigator with acutely ill oncology patients using strong clinical judgment and up to date oncology knowledge.
Ability to work flexible hours to accommodates research procedure and deadlines.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.