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Job description
Adagene Inc. is seeking a Head of Global Regulatory Affairs to lead global regulatory and quality strategies, oversee submissions to FDA, CFDA and other authorities, and guide cross-functional teams across clinical development, manufacturing and quality.
The role requires a PharmD or PhD with 10+ years in regulatory affairs, strong leadership, stakeholder management, and willingness to travel internationally, including to Suzhou, China.
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Worksite address
san diego, CA, 92189, US
Who can apply
Review the original listing for work authorization, qualifications and employer requirements.