625 data-"https:" "https:" "https:" "https:" "https:" "https:" "https:" "Newcastle University" positions at University of Pennsylvania
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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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operating supplies. Troubleshoot all assays and equipment when technical issues arise. Maintain sample logs and progess on assay runs. Analyze QC data from autoanalyzers. Label and collate assay results
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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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epidemiology studies, including but not limited to: a) understanding and interpreting data arising from observational research studies, managing and cataloging data output/findings, tracking the conduct
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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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. Discusses study design with research teams and applies bioinformatics tools to visualize, analyze, manipulate or interpret molecular data. May build and maintain databases for processing and analyzing genomic
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oversee all clinical visit activities including recruitment, enrollment, collection and processing of study data and biological samples, data entry and queries, and completion of monitoring and closeout
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to data collection, experiments, or studies; prepares materials and maintains research tools or resources. Helps manage project documentation and processes to ensure accuracy, compliance, and timely
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for all aspects of study coordination including subject recruitment, detailed data entry, collecting biospecimens, subject visits and follow-up and regulatory documentation. Job Description Job
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data into research databases containing patient/participant information • Assisting or leading in the preparation and submission of IRB documents Assist in the coordination of federally funded studies