Los Angeles, CA, USA
Under the direction of the unit Manager, you will function as a Study Coordinator within Clinical Trials in the Department of Urology.
In this role, you will work with the PI, Sub-Investigators, research personnel and hospital staff (collectively, the Study Team) to serve
as Study Coordinator and Data Manager for research studies by assuring compliance with all aspects of individual studies. You will be responsible for ensuring that protocol procedures have been completed accurately, safely, and in a timely manner. This includes the responsibility for research assessment and patient intervention under the supervision of the Principal Investigator (PI). All relevant regulatory and Good Clinical Practice (GCP) guidelines must be adhered to in addition to ensuring the timely coordination and completion of study related procedures for which the coordinator is responsible. Further, this position requires that you participate in patient recruitment and enrollment, data collection, source documentation, quality assurance, drug accountability and review, regulatory submissions of events as needed, protocol dissemination to health care professionals (via inservicescand meetings), patients and family members.
Under minimum supervision, you will set priorities based on research needs and requirements, completing responsibilities using university research regulatory guidelines. You will be expected to use judgment to determine most appropriate method of completing research projects.
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.
To apply, please visit the following URL:https://www.hospitalcareers.com/job/3866072/clinical-research-coordinator-urology/→