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. Summary of Essential Duties: Reviews and evaluates clinical protocols to assure the safe and optimal use of imaging devices. Conducts acceptance test on new equipment and timely physics survey for all
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the Rehabilitation team. Assists in the continuous quality improvement process, program development, administrative duties as assigned, and coordination of any student/intern/fellowship program, as requested. Assists
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education programs Educational Requirements: High School Diploma/GED Bachelors degree in science or related degree preferred Experience: 1-year clinical research related experience preferred Physical Demands
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external health care clinics that serve URMs to facilitate knowledge of clinical trials, process to refer patients for clinical trials, and early navigation to address barriers to clinical trials
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. Communicates with physicians and pharmacists to recommend changes in medication therapy to optimize patient outcomes (i.e. labs not at goal, discontinuation of medication). Supports the process of completing
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of the nursing process and the delivery of patient care for the specialty patient population. Provide personal nursing care and perform routine assigned tasks under the direction of a licensed Registered Nurse (RN
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education programs Educational Requirements: High School Diploma/GED Bachelors degree in science or related degree preferred Experience: 1-year clinical research related experience preferred Physical Demands
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, effectively adjusts priorities according to the workload and to meet the needs of the Division. Aligns to business and/or operations plans, contributes to process improvement, and participates in design and
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nursing process components and relevant interventions for direct and indirect Oncology patient care services that ensures the safety, comfort, personal hygiene, and protection of patients in a timely manner
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independently providing study coordination including screening of potential patients for protocol eligibility, presenting non-medical trial concepts and details, and participating in the informed consent process