126 data-"https:"-"https:"-"https:"-"https:"-"https:"-"https:"-"SciLifeLab" positions at City of Hope
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. · Work with investigators to assure the clarity and accuracy of data presentations. You will advise and assist with creation of clear, appealing data figures, model overview figures, graphical abstracts
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computational methods for cancer pangenomics using long-read sequencing data. Through TGen's Collaborative Sequencing Center (CSC), we have access to in-house PacBio Revio and Oxford Nanopore PromethION platforms
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candidate, you will: · You must have experience with flow cytometry, molecular biology techniques, cell culture, microscopy, tissue processing, immunohistochemistry, immunofluorescence, data analysis
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involves coordinating First in Human to Phase III and Investigator-Initiated Trials. Responsibilities include patient recruitment, informed consent, trial coordination, data management, and regulatory
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; and managing inventory and supply lists.Additional duties include assisting with specimen or data collection for research projects or demonstrations; cleaning and maintaining glassware and laboratory
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including study documents, research calendars, data collection tools, and its comprehensive financial system in an efficient and timely manner. This role will report to the City of Hope Director of Clinical
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protocols, while maintaining high standards of scientific rigor. Accurately record, analyze, and validate experimental data; generate figures and summaries to support ongoing projects and publications
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protocols to ensure efficiency and regulatory compliance while attending clinics as needed. You'll handle data compilation, registration, and submission, and maintain an effective system for data flow
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include not only operating the instrument but also assay development, sample preparation, calibration, data analysis, data management/backup and routine maintenance/trouble shooting. In addition, you will
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current and accurate protocol documentation; notify investigators of pertinent protocol changes. Maintain and complete regulatory documents for IRB, DSMB, and PRMC/CPRMC. Compile and submit data