87 computer-programmer-"https:"-"FEMTO-ST" "https:" "https:" positions at Medical College of Wisconsin
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, and monitor research studies. Within our Administrative Unit, the Clinical Research Operations Quality Program provides support such as regulatory guidance, budget support, research systems assistance
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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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academic medicine, and the continuous pursuit of knowledge, is at the center of everything we do at the Medical College of Wisconsin (MCW). In the role of Program Manager II you will work independently under
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academic medicine, and the continuous pursuit of knowledge, is at the center of everything we do at the Medical College of Wisconsin (MCW). As a Program Manager II - Kern National Network for Flourishing
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. Manages the division’s budget and resource utilization; prepares financial reports and projections for the Division Chief. Supervises administrative and program coordinator staff; ensures appropriate
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Experience: 4 years, Program/project coordination experience. Experience in philanthropy, non-profit, and/or creative agency setting Preferred Field: Graphic design, project coordination, administration Why
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or equivalent Two years patient care experience or graduated from an accredited Medical Assistant program #LI-AC1 Why MCW? 403B Retirement Package Competitive Vacation and Paid Holidays offered Back-Up Care Pet
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. Manages the division’s budget and resource utilization; prepares financial reports and projections for the Division Chief. Supervises administrative and program coordinator staff; ensures appropriate
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are essential to the scholarly mission of the mentor and host institution, and thus are expected to have the freedom to publish the results of their scholarship. Responsibilities Plan, design, and execute complex
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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