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Global Regulatory Affairs Lead – IND/NDA Submissions

KalVista Pharmaceuticals, Inc., Framingham

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A global pharmaceutical company is seeking an Associate Director of Regulatory Affairs. In this role, you will contribute to regulatory submissions to support the commercialization of products. Responsibilities include ensuring compliance and collaborating cross-functionally. Applicants should have a degree in a relevant field and at least 10 years of Regulatory Affairs experience, especially with FDA and Health Canada submissions. This position offers a dynamic work environment focused on innovative therapies.
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