216 department-for-translation-studies positions at University of California, San Francisco
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agencies; oversee study data integrity; implement and maintain periodic quality control procedures; interface with departments to obtain UCSF approval prior to study initiation; maintain all regulatory
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for the coordination of one or more single or multi-site, active or follow-up clinical trials; help prepare protocols for study initiation; help design flow sheets, data forms and source documents; gather and interpret
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Interpreter Services Full Time 78890BR Job Summary As a future member of the Interpreting and Translation Services Department, the candidate, under the direction of the Interpreting and Translation
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. Able to read & interpret data; translates data into meaningful information and uses data to shape work at both the department and enterprise level; possesses strong analytical and critical thinking
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on their size and complexity; act as intermediary between services and departments while overseeing data and specimen management; manage and report on study results; create, clean, update, and manage databases
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to advance mutual priorities. The final salary and offer components are subject to additional approvals based on UC policy. Your placement within the salary range is dependent on a number of factors including
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discovery and translation of drug properties. Communicate quantitative data, both internally and in the scientific community. Provide scientific and modeling leadership to research teams. Confidently conduct
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of one or more single or multi-site, active or follow-up clinical trials; help prepare protocols for study initiation; help design flow sheets, data forms and source documents; gather and interpret medical
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the management and coordinating the tasks of single or multiple clinical research studies, depending on their size and complexity; act as intermediary between services and departments while overseeing data and
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MED-CORE-INFD Full Time 79322BR Job Summary Senior Clinical Research Coordinators independently coordinate and are accountable for the overall administration of one or more clinical studies