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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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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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, procedural process, and recordkeeping. Computer, technical, interpersonal, oral communication, listening, and patience skills. Preferred Schedule: Full-time, Hybrid 95% Remote 5% Onsite Position Requirements
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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
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. Develop and distribute internal templates, memos, and announcements to keep staff informed about departmental activities and updates. Coordinate with central communications as needed to support external
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to prepare reports. Process payment requests, requisitions, and invoices. Distribute mail and organize filing systems accurately maintaining records. Use complex functions of a variety of computer applications
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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