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Our company is a global health care leader with a diversified portfolio of prescription medicines, vaccines and animal health products. + Participation in internal and joint internal/external research project teams relevant to the development of new compounds, and the further study of marketed compounds.
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Planning and managing GRPI interactions with our Research and Development Division's colleagues, regulatory liaison staff, and local regulatory affairs staff for submission of product applications and other related interactions with Health authorities.
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In BARDS (Biostatistics and Research Decision Sciences), a distinguished department within our company’s renowned Research and Development division, quantitative scientists, in partnership with other subject matter experts, apply state-of-the art scientific methodologies and tools to enable the discovery, development, regulatory approval, manufacturing, and marketing of medical drugs and vaccines for the benefit of patients and global human health.
$181,600 - $285,800 a yearFull-timeExpandApply NowActive JobUpdated 2 days ago - UpvoteDownvoteShare Job
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Execute regulatory strategies by leading the development, authoring and review of CMC submission components and documentation to support post-approval supplements/variations, annual reports, registration renewals and responses to health authority questions per established business processes and systems.
ExpandApply NowActive JobUpdated 6 days ago
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