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, preventing, and curing diseases, shaping the future of medicine through cutting-edge research. Responsible for manufacturing and isolating of human islets from pancreas donors under limited supervision
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, your primary responsibility revolves around upholding the integrity of data across various research studies involving human subjects. This involves tasks such as abstracting data, completing detailed
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to create impactful therapeutic interventions. Our diverse research scope extends from addressing health disparities in underserved human populations to studying naturally occurring cancers in canine and
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. As the Clinical Research Coordinator, your primary responsibility revolves around upholding the integrity of data across various research studies involving human subjects. This involves tasks such as
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Regulatory Coordinator at City of Hope, you'll play a crucial role in assisting our investigators with the submission of human subject research to regulatory committees, contributing to the advancement
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activation of human subject research to regulatory committees. This includes facilitating prompt submission of protocols, amendments, and updates to regulatory oversight committees and acting as the primary
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will: Ability to carry out cell culture experiments using transfection agents and RNA isolation to perform RT PCR experiments. Willingness to learn animal handling and testing with humanized mouse models
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, infectious hazards, radioactive materials, and radiation producing machines. Familiarity with federal and California regulations on human subjects research. City of Hope is an equal opportunity employer
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oncology therapies while working in a fast-paced environment. Trial responsibility ranges from First in Human and Phase I-Phase III clinical trials, in addition to Investigator Initiated Trials( IIT’s
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-doctoral fellowships), involvement with human observational or therapeutic studies, protocol design/writing for human sample, observational/retrospective or therapeutic studies. Familiarity with data