94 algorithm-development-"Multiple"-"Prof"-"Prof"-"Simons-Foundation"-"U.S" positions at Fred Hutchinson Cancer Center
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this position, the incumbent will develop novel computational tools to analyze TCR/BCR repertoire sequencing data & identify tumor-infiltrating lymphocytes with therapeutic potential. We are looking for a
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on managing colleagues to deliver on high priority projects and supervising daily operational work as well as core human resource responsibilities. The role will need to develop relationships with leaders
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program goals. For the GI Oncology Clinical Research Program: Advise program leadership and principal investigators on protocol development and selection by assessing clinical trial feasibility. Partner
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initiatives. Develop, edit, and maintain project administrative materials including project dashboards. Assist Sloan Precision Oncology Institute team members in administrative tasks related to research
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infections of varying severities. Define features of effective and ineffective antigen targets in the T cell repertoire and develop in vitro and in vivo models to test features of diverse immune specificities
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Processing Services Specialists, developing and maintaining relationships with other Fred Hutch departments and outside providers. Additionally, the role performs blood bank transfusion support and bone marrow
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environment researching the mechanisms of hematopoietic stem cell development and leukemogenesis. The focus of our lab is to unravel the dynamic intercellular interactions and signal pathways governing
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Li, operates at the intersection of statistics and biology to drive cutting-edge biomedical research. The JSB Lab focuses on developing statistical and computational methods motivated by important
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our South Lake Union campus. Responsibilities Primary/Essential Duties Provide administrative support for the Associate Vice President, Philanthropy, including meeting planning, material development
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in the development, implementation and management of clinical trials. Responsible for the collection, coordination, processing, and quality control of clinical trial data in accordance with protocols