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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
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for protocol eligibility, presenting non-medical trial concepts and details, and participating in the informed consent process. Responsible for accurate and timely source documents, data collection
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tissue, blood and urine, are stored along with selecting health information for later use in biomedical research. Researchers use the Biobank like a library, accessing samples with diverse genetic
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, evaluate, and apply cutting-edge computational and statistical methods and software for the analysis of biomedical and clinical data across the Cedars-Sinai enterprise. Are you ready to be a part of
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the commutable area. The Biostatistician II provides statistical services for Principal Investigators, clinical trials, and research studies. Performs statistical analyses, preparation of data sets and writing
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computer-based analyses of signaling pathways in human tumor samples, coupled with state-of-the-art technologies (single cell RNAseq and alike). Candidates are expected to be self-motivated, intellectually
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, microscopy, western blots, ELISA, histology, and manages related data analysis. The ideal candidate is independent, precise, and experienced with animal models and mammalian tissue culture. The individual will
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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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to assist in tasks supporting the coordination/implementation of noncomplex research studies. Supports objectives of research studies through noncomplex tasks such as data collection, prescreening
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/implementation of noncomplex research studies. Supports objectives of research studies through noncomplex tasks such as data collection, prescreening of potential and scheduling of current research participants