The individual’s primary functions will be to manage and lead aspects of pharmacoepidemiologic and reproductive epidemiology studies, including but not limited to: a) understanding and interpreting data arising from observational research studies, managing and cataloging data output/findings, tracking the conduct of statistical analyses described in observational research protocols and accompanying analytic plans, analyzing data, and drafting manuscripts; b) leading biomedical literature (i.e., systematic and scoping) reviews and synthesizing findings; c) completing institutional review board applications; d) completing data use agreement, data reuse agreement, and business associate agreement applications, and liaising with external groups (e.g., the Centers for Medicare and Medicaid Services) to execute these agreements; e) designing medical record abstraction forms and abstracting clinical data from primary medical records; f) managing conflict of interest reporting and data retention requirements; g) drafting research plan (e.g., data description, sample size) and technical sections of grant applications (e.g., protection of human subjects, inclusion of women, children, and minorities, research facilities and equipment), study abstracts, and manuscripts; h) drafting study progress reports; and i) generating data from publicly-available health statistics datasets (e.g., the Centers for Disease Control and Prevention’s National Center for Health Statistics). The individual will have secondary functions. These include: a) managing the Center for Real-World Effectiveness and Safety of Therapeutics' (CREST’s) summer program in target trial emulation and real-world evidence; and b) support CREST activities, including but not limited to managing its online presence. The latter requires a basic understanding of health communication and social media platforms.
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Job Type
Full-time
Career Level
Manager