Responsibilities

Play a key role in the delivery of world class patient care. Continuously elevate the quality of care within an award winning health system. Leverage your expertise to make a life changing difference. At UCLA Health, you can do this and more.

Under the direct supervision of the Director of Clinical Research and general supervision of the Vice Chair, Research within the Radiology Office of Research Affairs (ORA), the Clinical Research Coordinator (CRC) is responsible for managing the logistical and administrative aspects of clinical research studies. The CRC will function as a study coordinator across all assigned imaging-research programs, working closely with faculty principal investigators. The CRC will coordinate, manage and conduct clinical research studies in close collaboration with different departments (Modality directors/managers, contracts and grants management, etc.) to ensure compliance, safety and ethical conduct of clinical research trials.

Salary range: $23.04-$45.54 Hourly

Qualifications

• Ability to assist in the preparation of research presentations and manuscripts of publishable

quality.

• Ability to work a flexible schedule in order to meet changing priorities.

• ACRP or SoCRA or equivalent certification (preferred).

• College degree or clinical research experience or analytical experience; or an equivalent

combination of education and experience. (At least 2 years of experience in clinical research preferred)

• Demonstrated ability to organize, initiate and work independently to address responsibilities;

must have strong time management skills.

• 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.

• Experience in data management of clinical research protocols, including the completion of case

report forms and other study documents.

• Knowledge in FDA regulations (IND, IDE), ICH guidelines and Good Clinical Practice.

• Knowledge of the preparation of research regulatory documents, informed consents, and IRB

submissions.

• Previous experience in university-wide, state, and federal regulatory management in 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.

• Skill in organizing and maintaining accurate, up-to-date files and records for audits and other

follow-up activities.

• Skill in using computers; working knowledge of word processing, spreadsheet, database and

presentation programs.

• Skills in facilitating meetings with faculty, administrative-level professionals, research staff, etc.

from diverse backgrounds and different service sectors.

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.