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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
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journals to determine which are most appropriate for submission of a given manuscript. Proofread and edit documents to ensure accuracy. Administer data and research compliance duties. Extract and compile a
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to the director of the Neuromuscular Research Division, including scheduling and sending correspondence on behalf of the director and/or department. Compiles information, prepares reports, and is involved in
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, encumbrances, and projected balances. Provide faculty portfolio analysis and advise faculty on best practices for Pre Award , Post-Award management and Contracting. Compile financial information to process
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up to date to maintain accreditation and safeguard that missing or incorrect data does not prompt a site visit. Stay up to date on all regulatory standards and ACGME requirements. Compile and submit
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activities involved in the collection, compilation, documentation, and analysis of clinical research data. Participates in periodic quality assurance audits of protocols. Supports the development of study
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complex activities involved in the collection, compilation, documentation, and analysis of clinical research data. Monitor participants’ progress including documenting and reporting adverse events