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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
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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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information about Dr. Brown’s lab, please visit here. As a successful candidate, you will: Perform tissue culture using aseptic techniques for media preparation, cell passaging, maintenance, and
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assist others in the proper use of high quality computer operated microscope systems to include widefield, Confocal, and 2-photon microscope systems. As a successful candidate you will: · Train
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data obtained. · Lead the management of laboratory inventories, prepare stock solutions, handle and dispose biohazardous and non-biohazardous materials according to safety protocols when
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will also prepare data tables, figures, study schematics, model overviews, conference posters, podium presentations, and reference libraries. In addition, you will draft SOPs, IRB & IACUC applications
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, & Fri*** Performs all tasks related to the admission/discharge/transfer process for all patient types. Performs accurate collection of patient demographic and insurance information, to be verified upon
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will also prepare data tables, figures, study schematics, model overviews, conference posters, podium presentations, and reference libraries. In addition, you will draft SOPs, IRB & IACUC applications
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sequencing, metabolism, drug development, structural biology, and large-scale data analysis and computational biology. For more information about Dr. Deng’s lab, please visit here. As a successful candidate