682 data-"https:" "https:" "https:" "https:" "https:" "https:" "https:" "University of St" "St" positions at University of Pennsylvania
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candidates for research participation, conducting research visits, and ensuring the seamless flow of biological sample acquisition, data, and communications across translational research collaborations
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organization and implementation of a research study. The research coordinator will be responsible for all aspects of clinical trial coordination including: subject recruitment, detailed data entry, subject
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written communications Operationalize and oversee the data collection, archival and reporting of clinical trials metrics. Establish data collection methodologies, data validation, and the implementation
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images of selected objects; and other related information. Maintain records of completed exhibits. Participate in physical installation and deinstallation of exhibits as well as associated digital content
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, organize, process, store, and ship human biospecimens in accordance with approved SOPs and study protocols. Manage the biospecimen database, including creation and printing of sample labels, scanning, data
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. Live cell fluorescent microscopy and data analysis. Pouring plates and use of robotic pinner for genome-wide screening. Assisting in administrative duties for filing and compiling research grants
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suppliers. Will design, coordinate and perform reagent qualification and maintenance programs, monitor frequency of testing and resource availability, and track trend data and report results. The individual
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the data, maintaining research equipment and project resources. Experience with mouse models of tumor, cell culture, flow cytometry, PCR, and Western blotting are preferred. Prior work with immune cell
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numbers for Investigators. Coordinate the conduct of the research protocol. This includes maintenance of study documentation, data entry, source documentation and electronic case report forms, resolve data
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, timelines, and data management. Coordinates laboratory administration, compliance, and IRB submissions, and contributes to literature reviews, grant proposals, manuscripts, and study reports. May enroll