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renovations by identifying system capacity and constraints. Manage projects through the use of the FAMIS Computer Maintenance Management System (CMMS). Document and track all capital, and non capital projects
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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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population health data into program planning. Knowledge – Skills – Abilities Strong program/project management skills. Proficiency in Microsoft PowerPoint and Excel and familiarity with design software. Able
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completing medical physics residency program. Responsibilities: Assist with acceptance, commissioning, routine quality assurance, and post-service clinical verification of new and existing radiation oncology
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, heart bypass surgery, and heart attack State of the art equipment and new facilities due to billions of dollars in capital investment Access to an active transplant program with advanced therapies
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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
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of the program’s goals. Assist with recruiting, training, and supervising staff and managing the program budget. Primary Responsibilities Recruit, screen, enroll and obtain consent from program participants
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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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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