**Job Description**
**Join Cedars-Sinai and become part of a team that is at the forefront of medical advancements!**
Work alongside physician-scientists and researchers who are making life-saving medical and scientific breakthroughs. Our team of scientists develop some of the most advanced clinical trials in the world.
As a Clinical Research Coordinator II, you will work independently providing study coordination including screening of potential patients for protocol eligibility, presenting non-medical trial concepts and details, and participating in the informed consent process. The incumbent will be responsible for accurate and timely source documents, data collection, documentation, entry, and reporting including timely response to sponsor queries. The CRC II member will be responsible for compiling and reporting on each study including information related to protocol activity, accrual data, workload, and other research information. The incumbent will present information a...