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Global Modern Services, Inc. (USA) is looking for a seasoned professional in Global Regulatory Affairs. The ideal candidate will possess a PhD or Master's in the relevant fields and have over 8 years of experience in pharma/biotech R&D, specifically in regulatory affairs.
The role is based in California, with opportunities also in Spring House, PA, and Titusville, NJ. Candidates must demonstrate a solid track record in data product development and possess deep knowledge of submission pathways and industry standards.
This is a fixed-term contract position and may require some travel.