827 data-"https:" "https:" "https:" "https:" "https:" "https:" "Simons Foundation" positions at University of California, Los Angeles
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Administrator. Verify donor and recipient medical information to ensure organ and tissue compatibility. Review donor medical records to confirm consent, medical and social history, and relevant clinical
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also work with cultured cell lines, human clinical specimens and research animals. Other responsibilities include the preparation of data and technical writing for publications and grants and a
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consultation, answer questions regarding entitlements and provide information regarding available benefits. In this role, you will provide managers and employees with assistance throughout the leave lifecycle
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JOB DUTIES Description The Medical Scribe will provide medical record support services. Duties will include transcribing medical data quickly and accurately while patients are being examined
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concisely express ideas using appropriate vocabulary and spelling. Ability to relay information, either in writing or verbally, in a professional manner. Ability to independently resolve issues working within
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/review data for accuracy, completeness, and suitability Handle clinical trial administrative responsibilities Salary Range:$56.54-75.34/hourly JOB QUALIFICATIONS Qualifications Required: Current and valid
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University of California, Los Angeles | Redondo Beach, California | United States | about 2 months ago
, data-driven and ethical decision-making. commitment to CI-CARE vales and high emotional intelligence and team leadership. Salary Range: $86,400 – $184,800 Annual JOB QUALIFICATIONS Qualifications
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information clearly and concisely in a manner appropriate to the audience, whether oral or written. Actively listens to what others are saying to achieve understanding. Shares information with others and
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University of California, Los Angeles | Los Angeles, California | United States | about 2 months ago
problem-solving. Working under general supervision, the Administrative Assistant will manage non-routine tasks, handle sensitive and confidential information with discretion, resolve procedural issues
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of trial eligibility, enrollment, coordination of research visits, collection and management of participant source documents, regulatory submissions and file maintenance, data management, and specimen