Responsible for planning, designing, monitoring, coordinating, analyzing and producing scientific content and regulatory documents. Manages and reviews medical writing of study protocols, statistical analysis and study reports. Serves as a scientific resource for study teams and departments. Master's degree, specific professional/Doctorate degree preferred with 2 years of related experience. Under FLAS, incumbents in this position are exempt. PhD with > 3 years of experience in pre-processing and ...
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