Cedars-Sinai Clinical Research Coordinator I in Los Angeles, California

Summary of Essential Job Duties:

Clinical Research Coordinator I working with two division (Nephrology and IBD), providing coordination including screening of potential patients for potential eligibility, presenting non-medical trial concepts and details, and participating in the informed consent process. Responsible for accurate and timely source documents, data collection, documentation, entry and reporting including timely response to sponsor queries. Responsible for reporting on each study including information related to protocol activity, accrual data workload and other research information; present this information at regular research staff meetings. Strong interpersonal skills to facilitate communication with sponsors and study patients alike.Educational Requirements:

BA/BS degree required.

License/Certification/Registration Requirements:

ACRP or SoCRA (or equivalent) certificate preferred.


two years of directly related experience.

Physical Demands: (e.g., lifting, standing, walking)

Able to perform moderate lifting. Able to move between multiple locations (office and clinic space) to perform recruitment.