75 computer-programmer-"https:"-"INSA-toulouse" "https:" "https:" "https:" "https:" "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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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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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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. 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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files verification of enrollment. Prepares Candidate Background Assessment Program (CBAP) files for review and use in hiring decisions for clinical departments. Receives CBAP applications from candidates
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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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Qualifications: High School Diploma or equivalent 2 years medical assisting experience or graduated from an accredited Medical Assistant program. Required Certification: NRCMA (Nationally Registered Certified
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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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, 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