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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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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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rooms. Knowledge – Skills – Abilities Knowledge of biology, clinical judgment, medicine, cultural awareness, and consulting. Medical documentation, interpersonal, practice-based learning and improvement
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Position Description: As a Postdoctoral Researcher and according to the National Institute of Health (NIH) and the National Science Foundation (NSF), you will be an individual who has received a
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: Immunology, Biochemistry, Chemistry, Computational Biology, Biochemical Sciences or related Why MCW? Outstanding Healthcare Coverage, including but not limited to Health, Vision, and Dental. Along with
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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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activities via Computer-Aided Dispatch software. Coordinate radio communications between center and field-bas Assist in associate and executive protection details, investigations, special events security
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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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, 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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to detail in fast-paced, unpredictable critical care settings. Knowledge of quality control, customer service standards, information management, procedural process, and recordkeeping. Computer, technical