684 data-"https:" "https:" "https:" "https:" "https:" "https:" "https:" "Newcastle University" positions at University of Pennsylvania in United States
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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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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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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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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