651 data-"https:" "https:" "https:" "https:" "https:" "https:" "https:" "IFM" "IFM" "IFM" uni jobs at University of Pennsylvania
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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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market data for the job’s level. Internal organization and peer data at Penn are also considered. Equal Opportunity Statement The University of Pennsylvania is an equal opportunity employer. Candidates
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education as they directly relate to the requirements of the position, and in alignment with salary ranges based on external market data for the job’s level. Internal organization and peer data at Penn
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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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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
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enrollment, scheduling and follow-up, data collection, and regulatory documentation while collaborating closely with the CRU team. Position is contingent upon funding. This position is hybrid eligible after
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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