115 computer-programmer-"Multiple"-"U"-"Prof"-"Prof"-"U.S" positions at University of California, San Diego
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program. Analyzes and resolves operational problems of moderate scope. A complete application package will require a cover letter. Ability to use sound judgment in responding to issues and concerns
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of implementation of studies. The Clinical Research Coordinator (CRC) II will plan, develop and implement start-up procedures for multiple phase I-III research studies in assigned disease team as well as lead, direct
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. Ability to translate program planning into operational and fiscal requirements. Ability to advise department Chair, Vice-Chair, and PI’s on regulations and courses of action. Ability to weigh instructional
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medical charts and abstracting data from medical records. Knowledge of National Institute of Health (NIH), Good Clinical Practice (GCP), Injury and Illness Prevention Program (IIPP), Human Resource
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the research program. Responsible for providing the Principal Investigator with a written assessment of experimental outcomes. Participates in the planning of new and existing experiments, by studying available
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, and administers a full range of administrative operations in a small to medium academic department, or a small to medium non-academic department or program, where operations are significantly complex in
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of implementation of studies. The Clinical Research Coordinator (CRC) II will plan, develop and implement start-up procedures for multiple phase I-III research studies in assigned disease team as well as lead, direct
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Public Health professional degree program, an MS in Biostatistics, a BS in Public Health (BSPH, the only Health Sciences undergraduate program), an MAS in Leadership of Healthcare Organizations run in
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(public health and biostatistics), a Master of Public Health professional degree program, a MS in Biostatistics, the only Health Sciences undergraduate program (BSPH), a Master of Applied Science in
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of implementation of studies. The Clinical Research Coordinator (CRC) II will plan, develop and implement start-up procedures for multiple phase I-III research studies in assigned disease team as well as lead, direct