730 computer-programmer-"Multiple"-"U.S"-"Prof"-"Prof"-"O.P" positions at University of California, San Diego in United States
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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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, 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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knowledge of third-party payors including federal, state, and private health plans. Demonstrated computer skills/ability to work between multiple systems during calls. Ability to work in an interactive
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, fiscal management and administration of a full range of extramural grants, contracts, subcontracts, clinical trials funding, and service agreements from complex multiple Grants (direct and indirect
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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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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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. The Clinical Research Coordinator will plan, develop and implement start-up procedures for multiple phase I-III research studies in assigned disease team as well as lead, direct, and coordinator operational
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orders, following par levels Computer knowledge and skills to perform data entry of usage and waste tracking into online data base. Skill to interact and communicate positively with other staff, and
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assessment. Demonstrated experience with difficult beta testing and quality assurance for program/module enhancements and modifications to support complex financial aid business processes. Demonstrated testing
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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