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established protocols, while maintaining high standards of scientific rigor. Accurately record, analyze, and validate experimental data; generate figures and summaries to support ongoing projects and
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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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the research papers, protocols and organize data for grant application · Excellent communication skills, as the basis of internal or external collaboration Your qualifications should include
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-omics analyses. For more information on Dr. Wang, please visit here .
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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 each patient
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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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methods. Independently evaluate research data and initiate alternative approaches to improve the quality of results by providing input to overall research design that maximizes samples or refines the use
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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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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