642 data-"https:" "https:" "https:" "https:" "https:" "https:" "https:" "UCL" "University of London" uni jobs at University of Pennsylvania
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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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preferred. In addition to the above, the Research Specialist B should be able to plan and execute experiments with limited supervision. This individual should also be able to analyze and interpret the data
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; maintain inventory in the departmental biobank and Penn Medicine biorepository systems. Administer study questionnaires and collect survey data. Maintain accurate source documentation, study files and data
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, maintaining freezers and refrigerators) Data management tasks: maintain specimen inventory system(s) to ensure that the status of each sample is known, and documented including entering kit prep and processing
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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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. The Principal Investigator will design experiments with the applicant, but the applicant will be expected to troubleshoot these procedures as needed. The applicant will also keep accurate notebooks, perform data
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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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required by sponsor or Clinical Research Organizations (CROs) (i.e., case report forms and study binders) as directed by the supervisor. Conduct data entry in CRFs as provided by the study sponsor Organize