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, regulations, guidance, policy & procedure developed by the UChicago Institutional Review Board (IRB), Food & Drug Administration (FDA) Code of Federal Regulations (CFR), & the International Conference
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years before pursing graduate studies, although this can be extended by mutual agreement. Responsibilities Builds and manages data sets. Helps design research studies. Codes and implements statistical and
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responsibility for the following non-laboratory duties: transcribing and coding data; developing data collection instruments; presenting research; and recruiting and scheduling research subjects. Acquires higher
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forms; prepares abstracted/coded data for processing/analysis. Creates and/or updates case report form and/or source document templates. Coordinates reimbursement of subjects. Maintains inventory
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Practices (GCP) & all current local, state, & federal laws, regulations, guidance, policy & procedures developed by the Institutional Review Board (IRB), Food & Drug Administration (FDA) Code of Federal
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logic difficulties as necessary, under the direction of more experienced colleagues. Supports the IT development group in building new systems and enhance existing systems. Assists in coding, testing
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using the appropriate data management platforms, and enters and codes study data as needed. Maintains current training in research ethics through the Collaborative Institutional Training Initiative (CITI
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, quantum-engineering, and materials research lab spaces for sensitive lab equipment. Knowledge of building operations and building codes and building automation systems. Familiarity with general business
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experience as a Police Officer at the University of Chicago preferred. Technical Knowledge or Skills: Working knowledge of Illinois Criminal Statutes, Illinois vehicle code, local ordinances, and civil law
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. The duration of the hiring process is approximately 90-120 days. Technical Knowledge or Skills: Develop a working knowledge of Illinois Criminal Statutes, Illinois vehicle code, University rules and regulations