ResponsibilitiesUnder the direct supervision of the leadership of the lung Integrated Diagnostics (IDx) and the general supervision of the IDx Program Manager, the incumbent is responsible for managing the logistical and administrative aspects of the lung IDx program along with overseeing data management. Primary job duties of this incumbent will focus on lung imaging research, but may include other research programs depending on departmental needs. Qualifications* Experience in data management of clinical research protocols, including the completion of case report forms and other study documents. * ACRP or SoCRA ( or equivalent certification ) Preferred * RN Licensure, BA, MPH or other degree, or several years professional research or analytical experience; or an equivalent combination of education and experience. * Previous experience in university-wide, state, and federal regulatory management in clinical trials. Ability to supervise and train study coordinators and other staff or personnel involved in the conduct of research studies and clinical trials. Skill in analyzing information, problems, situations and procedures to define objectives, identify patterns and formulate conclusions. Skill in setting priorities which accurately reflect the relative importance of job responsibilities. Demonstrated ability to organize, initiate and work independently to address responsibilities; must have strong time management skills. Skills in facilitating meetings with faculty, administrative-level professionals, research staff, etc. from diverse backgrounds and different service sectors. Ability to assist in the preparation of research presentations and manuscripts of publishable quality. Effective interpersonal, oral, and written communication skills; knowledge of medical terminology; ability to effectively and clearly communicate research goals to faculty investigators, research team, support staff, etc. Demonstrated ability to interact diplomatically and sympathetically with a patient population in varying degrees of health. Demonstrated strong work ethic and dedication. Ability to work a flexible schedule in order to meet changing priorities. Knowledge of the preparation of research regulatory documents, informed consents, and IRB submissions. Ability to work closely and effectively with a variety of project personnel under a high level of stress. Skill in using personal computers; working knowledge of word processing, spreadsheet, database and presentation programs. Skill in organizing and maintaining accurate, up-to-date files and records for audits and other follow-up activities. 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.