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As a Research Associate I, your principle focus is the coordination of research studies including internal and external clinical trials from start-up to closure in collaboration with principal investigators and other members of the research team. You are responsible for the submission of ethics applications, consent/ assent forms, amendments, progress reports and other submissions to the Research Ethics Board. An integral member of the research team, you will integrate the knowledge and skills of data abstracting with the philosophy and standards of AHS and clinical trial sponsors.
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