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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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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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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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, customer service standards, information management, procedural process, and recordkeeping. Computer, technical, interpersonal, oral communication, listening, and patience skills Preferred Schedule: Position
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Position Description: Job Profile: Postdoctoral Researcher According to the National Institute of Health (NIH) and the National Science Foundation (NSF), a postdoc is an individual who has received
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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
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Position Description: Purpose Perform the day-to-day administrative activities of the clinical research trials program. Provide support to the team to facilitate the achievement of the program’s