127 programming-"https:"-"FEMTO-ST"-"UCL"-"https:"-"https:"-"https:"-"https:" positions at Cedars Sinai Medical Center
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programming languages such as Python or Matlab. Experience with in vitro and in vivo electrophysiological monitoring techniques and analysis. Ability to meet aggressive timelines and deliverables in a
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the Attending Veterinarian (AV), the Institutional Animal Care and Use Committee (IACUC), and Cedars-Sinai Medical Center (CSMC) research staff, in meeting CSMC's responsibilities associated with the program for
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at regular research staff meetings. May plan and coordinate strategies for increasing patient enrollment, improving efficiency, training of personnel, or identifying new research opportunities. Ensures
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. The Clinical Research Associate I works directly with a Clinical Research Coordinator, Research Program Administrator, or Research Nurse to coordinate and/or implement the study. Evaluates and abstracts research
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. Experience and Skills: Research laboratory experience is preferred. Understanding of general research objectives. Solid understanding of programming languages, neuroimaging tools, computing environments
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creative program. Project Scientists are not required to carry out independent research or to develop an independent research reputation and do not have teaching responsibilities. Ordinarily, the Project
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to generate research approach and analytic plans. Support process evaluation of a pilot smoking cessation program, including developing evaluation framework, creating and implementing a data collection plan
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regulations and applicable law. Participates in required training and education programs Qualifications Requirements: High School Diploma/GED required. Bachelor's Degree preferred. 1 year Clinical research
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for excellence in research! The Clinical Research Associate I/CPT works under the direction of a Clinical Research Coordinator, Research Program Administrator, Research Nurse, or other supervising staff to assist
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data analysis, hypothesis development, programming, troubleshooting, etc.). Organizes clinical/research trials in conjunction with the Principal Investigator and sponsor and/or funding source. Monitors