112 web-programmer-developer-"https:"-"UCL"-"U"-"P"-"https:" positions at City of Hope
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and clinical trials focused on advancing imaging modalities for the diagnosis and treatment of disease. Prepare, submit, and maintain regulatory (e.g., IRB) and budgetary documents for research studies
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small and long noncoding RNAs to the regulation of gene expression during development and functioning of the immune system. Besides being fundamentally important, this work can potentially shed light on
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quality control steps (e.g., concentration, fragment analysis) and troubleshooting of library preparation workflows. · Assay Development and Protocol Establishment: You will be required to establish
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successful candidate, you will: This project with Dr. Nagarajan Vaidehi involves developing and application of interpretable machine learning methods to uncover allosteric regulation of disordered regions in
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of complex biological data. Develops custom software and databases as needed. As a successful candidate, you will: · Consult on various research projects as assigned under supervision of the department
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folders Your qualifications should include: High School diploma or GED with evidence of progress or current enrollment in college, in an Associate’s or Bachelor’s degree program of study. 0-1 years
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visit here . If you are passionate about some of the following things, we are working on this may be the perfect opportunity: · Development of cell-free DNA (mutation and methylation), RNA, and
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autonomy. You will work with Cherng Center leadership to grow the research program and its educational offerings. You will serve as a project manager, navigating the regulatory review process for each
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pertinent clinical and protocol information on request forms. Develop and maintain knowledge of various aspects of processing specimens, with particular attention to safety practices. Identify and communicate
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and amendments to stay current with eligibility, treatment, and documentation requirements; develops study-specific QC and risk-assessment plans. Identifies clinical trial issues and quality risks