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Samuel Oschin Comprehensive Cancer Institute
The Clinical Research Office (CRO) has overall responsibility for the performance of cancer trials and other cancer research studies at the Samuel Oschin Comprehensive Cancer Institute and provides support and services to faculty and staff conducting oncology research. This includes coordination of staff support, provision of centralized systems, regulatory expertise, and quality assurance.
Centralized systems will be easily accessible through our website. These systems include a protocol library which will contain all active cancer-related protocols, a Protocol Review and Monitoring Committee online forum which will track documents and reviews, and a research manual with up-to-date documentation of standardized research procedures.
The CRO will maintain regulatory binders for Industry, investigator-initiated, and Cooperative Group trials in accordance with federal regulations. Common regulatory documents include the IRB approval letter, FDA Form 1572, CVs, medical licensure, and Financial Disclosure Forms. We have centralized resources and templates for providing commonly requested regulatory documents to Industry sponsors, drug manufacturers, and federal oversight agencies.
For more information, contact us at:
Cedars-Sinai Medical Center
8700 Beverly Blvd.
Los Angeles, CA, 90048