99 data-"https:" "https:" "https:" "https:" "https:" "https:" "https:" "University of Plymouth" research jobs at University of Maryland, Baltimore
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experience can be substituted for education. Prior laboratory work experience is preferred but not required. Basic computer skills with Microsoft Office programs. Hiring Range :$23.25-$24.93 per hour
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transplant. The position is responsible for assisting with coordinating the day-to-day operations of one or more research studies or clinical trial protocols. The position coordinates data collection and
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physically within the State of Maryland. Essential Functions - Clinical Research Assistant: Perform data collection by conducting research interviews. Recruit and screen subjects for research studies. Collect
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are expected to work primarily physically within the State of Maryland. Essential Functions - Clinical Research Assistant: Perform data collection by conducting research interviews. Recruit and screen subjects
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target trial emulation: Developing and Applying advanced causal inference methods to analyze real-world data (e.g., OLDW) Scientific writing: Publishing leading biostatistical and clinical journals Data
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of Maryland Baltimore and in the Baltimore area more broadly, as well as working with patients to describe the study to them, consenting participants, collecting study data, helping with study assessments
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participants, collecting study data, helping with study assessments, regulatory aspects of our studies, and possibly data analysis, literature reviews, and writing reports or manuscripts. Qualifications
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data and participate in biweekly study team meetings. The candidate must have an interest in health behavior research with older adults with dementia as they will spend the majority of their time working
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for Addiction Medicine. Benefits Information UMB offers a comprehensive benefits package that prioritizes wellness, work/life balance, and professional development, along with additional exciting perks
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coordinating clinical research patient visits and data collection. The position will support the conduct of clinical trials, including the coordination of start-up activities, scheduling and preparing