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: Job Duties: Conduct cell culture and rodent-based experiments. Compile, analyze, document, and draw tentative conclusions from experimental results. Confer with principal investigator to review work
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IRB maintenance tasks. Coordinate and manage assigned research studies’ collection, compilation, documentation, and analysis of research data. Assist with grant preparation and reporting. Implement
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coordination of complex clinical research. This position manages assigned clinical research studies by supervising a variety of complex activities involved in the collection, compilation, documentation, and
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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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, 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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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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with resident information, compile data, maintain and regulate access to resident's files. Support the program director in the management of the program budget – processing reimbursements, travel
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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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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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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