985 parallel-computing-numerical-methods-"Simons-Foundation" positions at University of British Columbia in Canada
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The Biostatistics/Informatics Junior Faculty Award is on hold for 2025. This award program was made possible by the Marilyn Hilton MS Research Fund. As part of our commitment to building a workforce
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at the Vancouver Campus of the University of British Columbia. This 1-year position with possibility of renewal will support a program of research on the evaluation of policies and programs designed to prevent work
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As of spring 2025, the Banting Postdoctoral Fellowships Program has concluded and is no longer accepting applications. As the most prestigious postdoctoral award in Canada, the Banting Postdoctoral
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Minimum Qualifications Completion of a relevant technical program or a university degree in a relevant discipline and a minimum three years of related experience or an equivalent combination of education
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. Researches and compiles information on products, equipment, services, productivity, work methods, etc.; analyzes labor and materials costs; recommends changes, policies and/or procedures to improve efficiency
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Update July 10, 2025: NSERC is longer accepting applications for the NSERC Postdoctoral Fellowship program. Please refer to the Canada Postdoctoral Research Award program web page for information
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laboratories across the country. Participants in the IC Postdoc Program have achieved numerous significant accomplishments, including: More than 450 articles in peer-reviewed journals Published in prestigious
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, prioritizes and responds to a variety of in-person, email, virtual or telephone inquiries from prospective and current students, LFS Program Directors or faculty, UBC departments and units, and the general
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inquiries from prospective and current students, LFS Program Directors or faculty, UBC departments and units, and the general public. Asks probing questions to determine what students really need, and refers
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a strong genetics community to develop and apply computational (bioinformatics) methods to improve diagnosis for individuals with rare genetic disorders caused by variations in genome sequences