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independent research including co-authoring papers and protocols Serve as statistician on clinical studies and trial protocols Develop, evaluate and make publicly available computer code following principles
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, shaping the future of medicine through cutting-edge research. The Analytical Development / Quality Control (QC) team at the Center for Bioinnovation and Manufacturing seeks a Quality Control Associate III
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collaborate with maintenance personnel to ensure uninterrupted facility operations. Enforce health and safety compliance. Personnel Development & Budgeting Interview and evaluate staff, ensure policy compliance
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profiling of mouse and human samples. Maintain accurate lab records, perform data analysis, and help prepare figures and publications. Assist with day-to-day lab operations, including preparation of reagents
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cell treatments. · Perform data analysis using statistical and computational methods. · Develop and implement mathematical models to understand and predict treatment outcomes
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oversee materials management, release of raw materials, drug substance, drug product and determination of final product disposition. · Develop quality/KPI metrics to support GMP activities and
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development utilizing viral vectors to contribute to an effort in developing neoantigen expressing vaccines for clinical investigations. The position is available as part of a multi-disciplinary research
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. The coordinator will prepare data tables and figures, study schematic and model overview images, conference posters, podium presentations, and reference libraries with minimal oversight by the PIs and Supervisor
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, amendments, continuing reviews, deviations, unanticipated problems and other reportable events. · Prepare materials for committee meetings for assigned protocol submissions ensuring completeness and
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, including calculations and graphical representations. Develop specialized skills in relevant laboratory research areas to support ongoing projects. Ensure strict compliance with safety protocols in material