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participants are appropriately registered and maintain documentation of participant registration. · Compile and submit data on appropriate forms according to protocol requirements. · Perform
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trial quality and regulatory compliance. This position works collaboratively with investigators, research staff, pharmacy, and leadership to identify compliance gaps through active data analysis using
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components—including study documents, research calendars, data collection tools, and financial modules. The CTMS Administrator collaborates closely with Clinical Research leadership, Legal, Finance, and other
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store blood samples following study and safety guidelines. Utilize EPIC and various sponsor web portals for study documentation and data entry. Perform other duties as assigned to support research
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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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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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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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: · 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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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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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