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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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Functions Recruit, screen, enroll and obtain consent from program participants. Conduct or coordinate training for program participants. Coordinate research protocols including arranging necessary
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Position Description: Every day, in ways both big and small, the Medical College of Wisconsin (MCW) is impacting lives for the better. MCW … changemaking for a healthier Wisconsin. As a Program
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the administrative needs of our investigators and research staff, and together we coordinate, regulate, and monitor research projects. Our Human Research Protection Program (HRPP) Office oversees
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clinics. Conduct or coordinate training for program participants. Travel to affiliate hospitals to recruit participants. Weekend coverage required. Coordinate research protocols including arranging
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information in Department’s triage software program. Answers incoming calls, takes appropriate complete messages and transfers to appropriate area. Documents in electronic medical record (Epic) and other
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and compose correspondence, reports, memoranda, and other documents using basic and more advanced functions of computer applications and software packages including OnCore, MCW’s Clinical Trial
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Informatics. Develop, implement, and maintain comprehensive databases and files related to program operations. Manage the execution of internal and external meetings, site visits, and special events as directed
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systems (Epic.) Coordinate multiple appointments efficiently for the program such as appointments for providers, chiropractors, physical and occupational therapy as well as procedures- using a patient
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research institutes. Engage in medical education by teaching medical students, residents, and fellows. Contribute to program development and growth within MCW’s Memory Disorders Program. Faculty rank will be