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conducts quality assurance on study data collected. Prepare, submit, and assist investigators with multiple levels of research documentation (i.e. IRB submissions, educational materials, reports, grant
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, interns, or trainees. Present research findings at meetings. Compliance Maintain accurate and up-to-date research records. Adhere to IRB, data security, and other compliance policies. Attend required
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, workshops, or speaker series. Familiarity with administrative data partnerships, IRB processes, or research compliance. Interest in and experience with responsible AI use in research or policy contexts
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to IRB and federal guidelines; Develops and implements policies and procedures; provides comprehensive direction to clinical research personnel; may participate in the hiring, training, and evaluation
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staff: Institutional Review Board (IRB), Scientific Review Committee (SRC), Radiation Safety Committee, Office of Research Quality Assurance (ORQA), Clinical Research Operations Office (CROO), Research
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of Authority logs Prepare and submit IRB documentation and support development of COI, DSMPs, and RDSPs Support study financial tracking, participant payments, and budget coordination Contribute to study start
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documentation, and regulatory submissions Communicate with IRB and support development of consent documents and regulatory materials Recognize when agreements (MTAs, CDAs, DUAs, DTAs) are required and coordinate
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dissemination materials. Support development and maintenance of a public-facing project website and dissemination strategy. Ensure compliance with institutional policies, IRB determinations, and sponsor reporting
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The Lab Manager (LM) provides administrative and research support for the Private Investigator (PI; Joan Orpella) and his lab (Orpella Lab; https://orpellalab.georgetown.edu/), housed in the GUMC
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Practice Documents (WPDs) Oversee and ensure completeness in appropriate AE and SAE reporting requirements as well as Deviation reporting to sponsors and the IRB. Manages the workflow by reviewing staff