582 computer-science-programming-languages-"St"-"FEMTO-ST-institute"-"ST" positions at Medical College of Wisconsin
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appropriately. Perform light typing / word processing as needed. Other duties as assigned. Knowledge – Skills – Abilities Knowledge of computers, clerical procedures, customer service standards, collaboration
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Position Description: Clinical Research Coordinator III - GOOD Study Purpose Coordinate the day-to-day administrative activities of the clinical research trials program. Provide support to the team
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for education on an equivalent basis Minimum Required Education: Master’s Degree or higher in Library and Information Science from an ALA accredited institution, or equivalent Minimum Required Experience
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leadership on higher education law, including tenure, FERPA compliance, Clery Act, admissions, financial aid/scholarship programming, student conduct/affairs and academic program administration, Leads drafting
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, speech pathologists, geneticists, psychologists, and social workers. This multi-specialty team concept was really the harbinger of things to come throughout medicine, as cleft care has existed as a multi
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) works as a member of a multidisciplinary health care team who will contribute to excellence in program administration, patient care, patient safety, research, quality improvement, and teaching. Position
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and case managers. The Advanced Practice Provider (APP) works as a member of a multidisciplinary health care team who will contribute to excellence in program administration, patient care, patient
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Consulting, which includes performing advanced administrative duties that require considerable skill, in-depth knowledge of organizational policies and procedures, managing dynamic calendars, initiating
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completing medical physics residency program. Responsibilities: Assist with acceptance, commissioning, routine quality assurance, and post-service clinical verification of new and existing radiation oncology
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of the clinical research trials program, including mentoring Research Regulatory Specialists, gathering regulatory documents, preparing review committee submissions, amendments and continuing review for human