611 computer-science-programming-languages-"St"-"ST"-"St" positions at Medical College of Wisconsin
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, adoption assistance, paid parental leave, tuition reimbursement program, and more! Medical College of Wisconsin The Medical College of Wisconsin (MCW) is the state’s only private medical school and health
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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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Practice Provider (APP) 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
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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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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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necessary for providing feedback related to proposals and coordinating resources. Tools & Technology – knowledge of desktop and mobile computers and technology as well as department specific analytical and
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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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Education: Bachelor’s Degree Minimum Required Experience: 5 years Preferred Education: Bachelors in Science Preferred Experience: 5 years of experience in research program coordination. Experience with
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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