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with Principal Investigators (PIs) and their research staff including but not limited to clinical research coordinators, research nurses, monitors, data coordinators, as well as the various committee
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panel development (20–40+ colors), data interpretation, and troubleshooting. Oversee operation, QC, and maintenance of flow analyzers, spectral cytometers (e.g., Cytek Aurora), and multi-laser sorters
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attend clinic as needed and play an active role in patient recruitment. You must be able to identify and extract pertinent data from the medical records and comprehend medical terminology and have
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. Skills in common RNA biology, epigenetics, and mouse models are preferred. The candidate should be self-motivated, with a proven track record of productivity. For more information about Dr. Yang lab
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regulating both normal physiology and pathogenesis. 2) Development of novel drugs to treat MASH, diabetes, and cancer. For more information on Dr. Wendong Huang’s research, please visit here . Your
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Human to Phase III and Investigator-Initiated Trials. Responsibilities include patient recruitment, informed consent, trial coordination, data management, and regulatory compliance. The position requires
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for accurately recording work performed including results and methodology. Calculate, compile and analyze data obtained from work performed. · Independently evaluate research data and initiate alternative
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for the quality assurance/control management of OnCore study calendar specifications and financial console data entry (parameters, protocol related, subject related, and milestones) ensuring alignment with
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establish and maintain relationships with patients, visitors and other hospital personnel, while assuring confidentiality of patient information · Compile and submit data on appropriate forms
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, this patient-facing role involves coordinating First in Human to Phase III and Investigator-Initiated Trials. Responsibilities include patient recruitment, informed consent, trial coordination, data management