551 data-"https:" "https:" "https:" "https:" "https:" "https:" "https:" "Fraunhofer Gesellschaft" positions at University of Pittsburgh
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. About the Library The Falk Library exists to: Nurture a love of reading and an appreciation of literature and stories. Help students develop the skills to find, evaluate, and apply information effectively
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, communicate with users, and walk to various campus locations. Must be able to lift and transport computer equipment weighing up to 30 pounds to various campus locations. The University of Pittsburgh is an equal
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, or data organization is a plus. Experience with animal research (e.g., mouse handling or tumor models) is desirable but not required. Job Summary Performs a variety of independent laboratory work and
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. The incumbent will follow established protocols, troubleshoot protocols as necessary, and collect and analyze data. Much of the work will be conducted at either BioSafety Level-2 or at BioSafety Level-3 in
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experimental protocols and analysis of experimental data. The candidate will be responsible for performing other laboratory techniques such as DNA/RNA extraction, histology, immunostaining, western blots, flow
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bioinformatics analyses of existing RNA sequencing datasets, bench-based experiments using animal models, primary cells, and human tissue. Physical Effort Must be able to sit, stand, and use a computer for
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inventory and assists with ordering. Essential Functions Duties include assisting with animal experiments, tissue processing, molecular and histological assays, data collection and organization, and general
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for participation or continued participation after enrollment with exception from informed consent, and reliably ascertains primary study outcomes. Completes accurate data collection, audits research studies
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written communication skills. The Conflict of Interest Committees Program Manager will work independently after receiving information and guidance from the Director of the COID. Job duties include, but
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-Marie Lavenburg. Candidate will recruit research participants for clinical trial including conducting the informed consent process (over the phone). Complete data collection for study visits and enter