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Regulatory Affairs Specialist: Global Submissions

Katalyst CRO, Richmond, Illinois, United States, 60071

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A leading clinical research organization is seeking a Regulatory Affairs professional to support compliance with FDA and EU regulations for product development. The role involves coordinating regulatory filings, developing strategies, and representing the company with regulatory agencies. Ideal candidates will have a bachelor's degree and experience in Regulatory Affairs or a related field, along with proficiency in Microsoft Office applications. #J-18808-Ljbffr