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of pediatric IBD and celiac disease! The CRCA will coordinate complex aspects of multiple clinical studies and work under the general direction of multiple principal investigators and/or supervisor
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of the principal investigator to oversee and direct clinical course of research participants in clinical trials. Assess physical health and administer treatments throughout the study aligned with scope of practice
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on experimental design and/or research direction to principal investigator. Independently conduct complex (lab and/or field) experiments to gather data for a portion of a major research project. Interpret and
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objectives are met. The ADD will assist and advise the Division Chief, ensure compliance in all functional areas (i.e., Finance, Human Resources, Research Administration, Clinical Administration, Facilities
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: https://med.stanford.edu/anesthesia.html Duties include: Independently conduct a portion of the research project(s). Make recommendations on experimental design and/or research direction to principal
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conceptual approach. · Build and organize data as requested by principal investigator or supervisor; use common statistical programs requiring the application of job control language in generating and
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records of experiments and outcomes. General computer skills and ability to quickly learn and master computer programs, databases, and scientific applications. Ability to work under deadlines with general
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*: Serve as primary contact with research participants, sponsors, and regulatory agencies. Coordinate studies from start-up through close-out. Determine eligibility of and gather consent from study
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participant management and study procedure completion, while maintaining regulatory compliance. Duties include*: Serve as primary contact with research participants, sponsors, and regulatory agencies
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the National Human Genome Research Institute (NHGRI). The IGVF Consortium aims to understand how genomic variation affects genome function, which in turn impacts phenotype. The IGVF DACC's primary task is to