609 programming-"the"-"DAAD"-"U"-"IMPRS-ML"-"UCL"-"FEMTO-ST" positions at Medical College of Wisconsin
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are committed to fostering an inclusive community of outstanding faculty, staff, and students, as well as ensuring equal educational opportunity, employment, and access to services, programs, and activities
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to state-of-the-art facilities and resources. Supportive and collaborative work environment. A competitive 403(b) retirement plan with an 8% employer contribution. Generous CME allowance to cover societal
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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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well as ensuring equal educational opportunity, employment, and access to services, programs, and activities, without regard to an individual's race, color, national origin, religion, age, disability, sex, gender
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development. Establish an individual development plan (IDP) that incorporates equally the postdoc's career and training goals and the mentor's research goals. Pursue basic, or translational projects so long as
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our exciting program in human neuroscience. Primary Functions • Assist with design and implementation of experimental techniques and software analysis techniques for conducting efficient
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Program in a variety of clinical settings, working closely with an attending physician to care for pediatric patients in a hospital-based Child Advocacy Program at Children's Wisconsin and outpatient Child
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community of outstanding faculty, staff, and students, as well as ensuring equal educational opportunity, employment, and access to services, programs, and activities, without regard to an individual's race
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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