64 computer-programmer-"Multiple"-"U.S"-"Prof"-"O.P"-"Humboldt-Stiftung-Foundation"-"UCL" positions at Medical College of Wisconsin
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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
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the direction of the faculty member serving as the Program Director or designee to oversee the coordination, training and technical assistance, research, analysis, and program evaluation needs for multiple public
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students to Pain Fellow and Psychology graduate student. The program serves multiple sites both near the Froedtert and MCW campus, as well as several community sites and covers both ambulatory and in-patient
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Position Description: In the role of Program Coordinator III - Performance Reporting & Practice Analytics, you will beworking in the Medical College Physicians Administration. Under
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to develop new ideas by analyzing complex, multi-faceted information. Ability to prioritize multiple assignments and deadlines. Technical knowledge of FERPA, F-1 visa regulations and J-1 program
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within the Medical College of Wisconsin (MCW) and be inspired by the work we can do together to improve health, and make a positive, daily impact in our communities. As a Program Manager I - Annual Giving
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Functions Serve as program assistant for Center projects. Aid on multiple active grants at CAPS as needed. Perform data collection during participant visits. In collaboration with the PI, lead recruitment
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education: Student must be in good academic standing in a bachelor’s level program or in a graduate level program in communications, journalism or related field. Minimum experience: Experience writing
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will work under the general direction of the Program Manager of Workforce Development. An ideal candidate is a forward-thinking professional with technical expertise and the ability to collaborate with
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, amendments, protocol deviations, serious adverse events, continuing progress reports, and informed consent documents. Following IRB guidelines, draft and/or modify documents as required by research program