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, and WHODrug). Awareness of common data elements for research and understand how they would be applicable to their protocol(s). Maps a protocol's data flow plan including data capture, storage, transfer
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updating reports on study progress for the PI and other study team members and collaborators. Science: Assists with simple literature searches. Under guidance, develops elements of research protocols
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updating reports on study progress for the PI and other study team members and collaborators. Science: Assists with simple literature searches. Under guidance, develops elements of research protocols
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projects and quality improvement initiatives Provides oversight of transplant staff education for critical elements of medication use in patient care and clinical research Educates medical, nursing, and
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population. Ensure the availability of accurate and appropriate patient/family education materials. Facilitate electronic capture of data elements required for the stroke program and to improve the care
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periodically trained in new elements of the Compliance Program, and performance will subsequently be evaluated in part according to adherence to compliance rules. Supervision Responsibility The Associate Vice
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standards should be used in creating eCRFs and EDCs and integrates as according to best practices (E.g. IDC 10, CDISC, MedDRA, and WHODrug). Awareness of common data elements for research and understand how
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small group meetings. Assist senior members (graduate students, postdoctoral fellows, technicians, and staff scientists) in various lab activities. Primary activities will be observation, scribing, sample
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updating reports on study progress for the PI and other study team members and collaborators. Science: Assists with simple literature searches. Under guidance, develops elements of research protocols
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, if applicable. Prepare, coordinate and review proposal elements such as biosketches, justifications and facilities & resources for consistency, accuracy, and completeness. Monitor compliance with agency and