657 data-"https:" "https:" "https:" "https:" "https:" "https:" "https:" "Univ" positions at University of Pennsylvania in United States
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, analyze data, and present findings. Preferred qualifications for this position include expertise in handling and processing primary clinical samples, genetic engineering using viral or non-viral delivery
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regulatory obstacles to activation, and propose improvements to the process will track, analyze and report to senior leadership department-wide trial characteristics, accrual information and audit/monitoring
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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 are also considered. Equal Opportunity Statement
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salary ranges based on external 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
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completion of project/program deliverables. Job Description Job Responsibilities Drive a research project (collect, analyze and interpret data, and present data at group meetings) Help in the general running
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ensure adherence to protocol requirements Organize and maintain all required documentation- including source documentation, case report forms, and research charts. Collect, review and report study data
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on the candidate’s qualifications, experience, skills, and 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
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research area. Coordinate the screening of patients, subject enrollment, collection and storage of biological samples and related study documents, and collection of clinical data. Assist with Institutional
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based on the candidate’s qualifications, experience, skills, and education as they directly relate to the requirements of the position, and in alignment with salary ranges based on external market data
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for the abstraction of complex medical data in order to determine study eligibility. Manage data using different tools, systems and statistical software package and submit protocol modifications and continuing reviews