1,593 data-"https:"-"https:"-"https:"-"https:"-"https:" positions at University of Michigan
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, such as changes in airway/breathing, heart rate, acute change in level of consciousness, seizure etc. Effectively communicate with patients to obtain important clinical information, instruct the patient
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. Learn more about the work modes . Additional Information This job posting is for a University of Michigan Temporary position. Temporary employment may be full or part time, but in either case is limited
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and Regulation Clinical Study Operations (GCPs) Study and Site Management Data Management and Informatics Leadership and Professionalism Communication and Teamwork Mission Statement Michigan Medicine
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, preparing area activity and financial metrics for data reporting. Maximize work efficiency through the use of computers and other technologies as evidenced by proficient skill in accessing and entering
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reconciliation documentation, form(s) preparation, relevant screenings, following predetermined protocols and other tasks as assigned. May obtain medical records and prepare medical information and reports
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approaching pregnant and laboring women for recruitment, obtaining informed consent, collection and recording of data and supporting research providers. This position is .8 FTE (80% or 32 hours a week) and
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procedures, systems, events, and logistics. Data-Driven Insights & Market Intelligence (10%) Partner with CDO colleagues and leadership to collect, interpret, and communicate employer and market data. Use data
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provide coordination for clinical research projects such as registries, retrospective data reviews, studies in long-term follow-up, and other non-interventional studies. Responsibilities* Knowledge of all 8
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vision coverage effective on your very first day 2:1 Match on retirement savings Responsibilities* Oversee UH Front Desk Operating Room clerical tasks Schedule add-on cases in the OR Computer System Move
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.Scientific Concepts and Research Design 2.Ethical Participant Safety Considerations 3.Investigational Products Development and Regulation 4.Clinical Study Operations (GCPs) 5.Study and Site Management 6.Data