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responsible for the implementation of their assigned portfolio of clinical studies, including regulatory submissions, data abstraction/entry/management, participant screening and enrollment, and study
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, please visit the Office for Equal Opportunity Compliance website for general information about requesting accommodations , as well as information about requesting accommodations specifically
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study team members by participating in recruitment and selection of study participants; document and collect data to support protocol screening and determine compliance with eligibility requirements
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informed documents, and record data collection according to the study research protocol. This position reports to the study Principal Investigator and works in collaboration with other research specialist
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The Research Enterprise Applications Lead, University Information Services, Georgetown University, will contribute to the ongoing strategic direction of Research Technologies and its service portfolio
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include: collecting and analyzing data to identify underlying social and economic problems, and evaluating the effects of existing policies and government programs. Incumbent completes robust research and
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visitor passes, and enforcing parking and safety regulations to support space availability and public safety. Provides information and assistance to visitors and members of the Georgetown Law community
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, clinical and other community settings as required. Collect and manage specimens and clinical data in accordance with study protocols. Educate and advocate for research participants, ensuring informed consent
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implementation of standard operating procedures, control procedures, and schedules monitoring activity and usage patterns in support of Internal Audit and identifying potential elements of fraud serve as a data
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hub for critical, timely information about health policy litigation. The Director will also be responsible for advancing the mission of the O’Neill Institute, including supporting the leadership team as