281 master-"https:" "https:" "https:" "https:" positions at University of Pennsylvania
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, bioinformatics pipeline development, and computational analysis of large-scale biobank datasets to study cardiovascular disease genetics. Primary responsibilities include analyzing common and rare genetic
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diseases. The primary function of this position is to facilitate, promote, and ensure the conduct of high-quality clinical research in accordance with Good Clinical Practice (GCP), institutional policies
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of experience or equivalent combination of education and experience is required. Experience in lab management and/or research support and Masters degree preferred. Job Location - City, State Philadelphia
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Computing (HPC) Systems Engineer to join the team. PARCC's main cluster (Betty), delivers HPC, data-intensive science and Artificial Intelligence (AI) resources to researchers at the University
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Research Coordinator A Job Profile Title Clinical Research Coordinator A Job Description Summary The CRCs primary position will be to recruit patients at the University of Pennsylvania for ACCELERATE-PACE
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of overall strategic plan for the department. Collaborate with on-campus fund-raising staff, including colleagues in central development office (Principal Gifts, Leadership Gifts, Major Gifts, Planned Giving
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globally, and overseeing material transfers, IRB, and IACUC submissions. The ADAF will report to the Director of Division Administration for GI and have an indirect reporting relationship the Chief Research
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to support data collection and analysis for clinical epidemiology research in pediatric oncology. Working under the direction of the Principal Investigator (PI), the individual will provide support for
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of experience or equivalent combination of education and experience is required. Master's degree in Public Health, Social Sciences, Social Work other relevant field from an accredited institution of higher
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Team Leaders and Principal Investigators with initiating study procedures for new IITs and industry-sponsored clinical trials. Manage all aspects of Phase I – IV clinical trials. Participate in