149 computational-physics "https:" "https:" "https:" "https:" "Univ" positions at Cedars Sinai Medical Center
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resistance and bacterial pathogenesis, as well as potential therapeutic targets for these hard-to-treat infections. Experience with bacterial genetics, infection models, and computational biology are desirable
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Project Scientist (Time-resolved Fluorescence Spectroscopy) - Butte Lab - Department of Neurosurgery
of time to contribute high-level skills to a specific research program. This role is not required to carry out independent research or to develop an independent research reputation and do not have teaching
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. Develop hypothesis and assist in planning steps for the investigative process. Review and remain current on literature as it relates to clinical and research studies. Coordinate all lab and clinical
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one of the top hospitals in California and in the nation by U.S. News & World Report. As the Scientific Director of the OncoBiobank and appointments at the Computational Medicine and Pathology
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of research participants for protocol eligibility, presenting non-medical trial concepts and details, and participating in the informed consent process. The CRC I member is responsible for accurate and timely
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and details, and participating in the informed consent process. The CRC II member is responsible for accurate and timely source documents, data collection, documentation, entry, and reporting including
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program. The lab has a strong track record of translating mechanistic bench science—including studies that interrupt signaling between the tumor and host—into clinical trials across multiple cancer types
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, Research Program Administrator, Research Nurse, or other supervising staff to assist in tasks supporting the coordination/implementation of noncomplex research studies. Supports objectives of research
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Cardiology at Cedars-Sinai and has led the clinical program and trained over 50 fellows both from within the United States and internationally. What will you be doing in this role? Working independently but in
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screening of potential patients for protocol eligibility, presenting non-medical trial concepts and details, and participating in the informed consent process. Responsible for accurate and timely source