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, compilation, documentation and analysis of clinical research data. Participate in periodic quality assurance audits of protocols. Assist with study budgets and contracts and assist with grant applications
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planning, policy making and program evaluation. Compiles information, prepares reports and is involved in implementing departmental policies. Job Description: Key Roles and Responsibilities: Serve as the
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the overall clinical study coordination of clinical research. This position manages assigned clinical research studies by supervising a variety of complex activities involved in the collection, compilation
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manages assigned clinical research studies by supervising a variety of complex activities involved in the collection, compilation, documentation, and analysis of clinical research data. Monitors
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Director by performing fact-checking, managing references, and compiling information to assist with grant applications. Job Description: Key Roles and Responsibilities: Conduct fact-checking for various
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research. The Clinical Research Coordinator will manage clinical research studies by coordinating and participating in a variety of complex activities involved in the collection, compilation, documentation
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research. The Clinical Research Coordinator will manage clinical research studies by coordinating and participating in a variety of complex activities involved in the collection, compilation, documentation
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the RDO Director, PIs, Co-Is, and partner institutions. Oversee the process of compiling application documentation such as biosketches, letters of support, human subjects section documents, budgets/budget
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to obtain data for research purposes; compile, analyze, document and draw tentative conclusions from experimental results. Job Description: Job Duties Outlined Perform routine laboratory techniques and
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technical duties involved in conducting physical, chemical, biological and other research laboratory tests, experiments and determinations to obtain data for research purposes; compile, analyze, document and