111 data-"https:"-"https:"-"https:"-"https:"-"https:"-"https:"-"https:"-"U.S" positions at City of Hope
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research studies. Compilate, register and submit study data. Monitor project databases and maintain a system of effective data flow associated with research protocol(s). Facilitate and manage multi-faceted
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extensive review of case report forms and study data, utilizing medical records, laboratory data, transfusion services records, and any other source used to produce study data. Generates an audit report or
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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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. · 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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: · Perform collaborative research with multiple faculty members at ARDMRI on projects involving genomics data analysis using single cell RNA-seq, CHIP-seq/ATAC-seq, spatial transcriptomics, HiC/HiCHIP, RIBO
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support of leukemia genomics and other biomedical research projects. The position emphasizes next-generation sequencing (NGS) data analysis, workflow development, high-performance computing, and structured
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compliance. Work on data abstraction and analysis. Interface with existing institutional resources/teams, including Posiedon, Honest Broker, STATA, RedCap, Excel, and others. Download and manipulate data from
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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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research protocols to assure efficiency and regulatory compliance of the protocol, attending clinic as needed. You will be responsible for compilation, registration and submission of data; monitoring study