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, legal agreement and other documents requiring the compilation, analysis and evaluation of data. Review documents received for supervisor; check and compare with source documents and bring significant
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communicate updates to appropriate staff. Maintain management and procedural manuals, records, reports, correspondence, and other office documentation. Compile, summarize, and analyze data to support weekly
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of consent plans and documents for participants. Under supervision, develops and submits documentation and information for IRB review. Assist with the compilation of documents needed for regulatory and safety
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accordance with University policies and sponsors' requirements regarding records, reports, controls, and conditions governing expenditures of funds. Coordinate, compile, and prepare operational and financial
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) or similar Clinical Research Unit (CRU), Oversight Organization (OO) designee. Participates in day to day operations related to the collection, compilation, and documentation of clinical research data and may
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for research purposes; compile, analyze, document and draw tentative conclusions from experimental results. Confer with principal investigator to review work assignments and develop plans for research
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. Assist with preparation of reports, proposals, briefing materials, reference documents, and informational resources requiring research, data compilation, analysis, and evaluation. Support financial
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, chemical, and biological experiments to generate and analyze data. The person compiles results, draws preliminary conclusions, and collaborates with a principal investigator to plan experiments and refine
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equipment as well as coordinating food. Summer School Support Collaborate with the Director to compile instructor lists for Summer Session Term I and Term II. Work with the Director to determine summer
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semi-annual evaluations process of all trainees directly involved with trainee education. Design and administer the program's educational curriculum and compile necessary data for continuous quality