620 computer-programmer-"https:"-"Inserm" "https:" "https:" "https:" "https:" "UCL" "UCL" "UCL" positions at University of Pennsylvania
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significant experience with mouse preclinical models to contribute to our dynamic team. The successful candidate will oversee daily operations of the research program including mouse colony breeding and
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program required. Certification preferred. 1 to 2 years of experience or equivalent combination of education and experience is required. Experience with venipuncture, finger stick, laboratory procedures
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equipment necessary for clinical lab research and program support. Process non-PO payment and Concur expense reimbursements, providing support and guidance to Faculty and Delegates. Process service provider
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connection with the legal adoption of an eligible child, such as travel or court fees, for up to two adoptions in your household. To learn more, please visit: https://www.hr.upenn.edu/PennHR/benefits-pay
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, visit www.wharton.upenn.edu. The IT Technical Director for Wharton will lead instructional technology efforts under Wharton Computing's IDEA Courseware brand. This role provides strategic leadership
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program logistics. Coordinate with the Executive Director of Development to support donor-facing presentations and strategic fundraising communications. Collaborate extensively with Organizational Impact
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connection with the legal adoption of an eligible child, such as travel or court fees, for up to two adoptions in your household. To learn more, please visit: https://www.hr.upenn.edu/PennHR/benefits-pay
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including personal computer, photocopier; demonstrated typing skills; familiarity with an academic medical environment is preferred. Job Location - City, State Philadelphia, Pennsylvania Department / School
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authorities, Sponsors and cooperative groups as directed by the ACC CRU Research Team Program Manager. Be actively involved in planning and implementation of patient recruitment into studies (involves deciding
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but will include the following: This individual will work independently with minimal supervision Communicate and liaise with regulatory bodies, such as the IRB, ClinicalTrials.gov, and the PCORI program