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multidisciplinary investigators, clinical study teams, data managers, and regulatory professionals while contributing to study design, statistical analysis, scientific reporting, and publication
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of this position are the following: Recruits, consents, and retains study subjects. Collects clinical data from subjects and/or medical records. Assists in the creation and management of documents
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. Develops, implements, and maintains data management protocols in the R and SAS computing environments (and other statistical software depending on project needs) to clean, manage, and merge
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experience supervising or mentoring other scientists. Certifications/Licenses N/A Required Knowledge, Skills, and Abilities Experience with high-performance computing, data management, and shell scripting
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experience supervising or mentoring other scientists. Certifications/Licenses N/A Required Knowledge, Skills, and Abilities Experience with high-performance computing, data management, and shell scripting
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student records and systems highly preferred. Equipment Utilized Desktop and mobile computing devices. Microsoft Office software applications (Excel, Access, PowerPoint, Word). Email and Calendaring
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. The Postdoctoral Associate will assist with scientific and operational aspects of ongoing studies. Responsibilities may include finalizing study protocols; developing manuals of operations and
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), Environmental Analysis and Communication Group ( EAC ), Center for Energy Environmental and Economic Policy ( CEEEP ), and Bloustein Center for Local Government Research. This merger creates strong
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study protocols; developing manuals of operations and training materials; preparing, submitting, and maintaining IRB documentation; coordinating with domestic and international collaborators; and
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study protocols; developing manuals of operations and training materials; preparing, submitting, and maintaining IRB documentation; coordinating with domestic and international collaborators; and