Global Regulatory Submissions Lead
Listed on 2026-10-09
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Management
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IT/Tech
Artiva Biotherapeutics Inc. is seeking a Senior Director of Regulatory Affairs to lead regulatory submissions and strategy for global programs on the cell therapy platform.
You will prepare CTDs, IBs, and clinical protocols while ensuring compliance across U.S., EU, and other major markets. Ideal candidates bring 10+ years in regulatory affairs within cell or gene therapy, with leadership experience and a track record in late-stage development.
We are seeking a motivated Global Regulatory Submissions Lead to join Artiva Biotherapeutics Inc. in San Diego, CA, United States.
Consider building your career as a Global Regulatory Submissions Lead at Artiva Biotherapeutics Inc.
The Global Regulatory Submissions Lead position in the Legal, Management & Operations field is open for applications.
We have an opening for a Global Regulatory Submissions Lead in San Diego, CA, United States within Legal, Management & Operations.
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