1,983 data-"https:" "https:" "https:" "https:" "https:" "https:" "https:" "The University of Gothenburg" uni jobs at University of Michigan
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at Michigan Medicine. You'll collect, organize, and analyze data to help leaders make informed strategic decisions and improve clinical processes. You'll design dashboards and reports, and ensure data is
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-day management of research operations, including coordinating data collection for EMA and longitudinal studies, managing IRB protocols, overseeing participant recruitment and scheduling, supporting data
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research that together enhance our contribution to society. Job Summary Interview patients to obtain/verify correct mailing address, phone numbers, other personal/demographic information, emergency contacts
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to confidential information; therefore, the workspace should provide adequate privacy to protect sensitive information. Equipment, including a laptop and monitors, will be provided for your use. Occasional overtime
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information, emergency contacts, primary-care physician, the person who is financially responsible for their outstanding balances (guarantor), and insurance information. Enter all information into the Michigan
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Apply Now Responsibilities* Assist with cleaning, harmonization, aggregation and analysis of clinical data for a large ophthalmology repository. Extract information from unstructured electronic
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monitoring data accessible to the public by developing a website and automating data updates. The assistant will help build a user-friendly platform that shares sensor readings, connect hardware data streams
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completion Creates and manages recruitment and enrollment tracking logs for multiple studies 25% Data Coordinator Responsibilities: Completes complex CRFs in accordance with ALCOA-C principles during study
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claims data, survey data, and qualitative data generated through interviews or focus groups; responding to media and legislative staff inquiries; monitoring relevant policy activity at the state and
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studies and clinical trials. Performs study visits including pre-visit preparation, data and biosample collection during visits, shipping of materials and data entry. Arranges follow-up protocol study