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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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health, health sciences) Preferred experience: 8 years of clinical or cardiovascular (CV) experience, ideally with direct involvement in care delivery, clinical program development, or quality improvement
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, & more. A competitive 403(b) retirement plan with an 8% employer contribution. Qualifying employer in the Public Service Loan Forgiveness (PSLF) program, offering eligible employees the opportunity
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• Organize clinical program patient and study participant charts and files, and distribute to appropriate locations • Collect required data from study coordinators and enter onto clinical research forms and
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to detail in fast-paced, unpredictable critical care settings. Knowledge of quality control, customer service standards, information management, procedural process, and recordkeeping. Computer, technical
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to detail in fast-paced, unpredictable critical care settings. Knowledge of quality control, customer service standards, information management, procedural process, and recordkeeping. Computer, technical
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to detail in fast-paced, unpredictable critical care settings. Knowledge of quality control, customer service standards, information management, procedural process, and recordkeeping. Computer, technical
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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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rooms. Knowledge – Skills – Abilities Knowledge of biology, clinical judgment, medicine, cultural awareness, and consulting. Medical documentation, interpersonal, practice-based learning and improvement