Global Regulatory Lead, Rare Disease Programs (NDA/BLA)

Job description

GondolaBio in Palo Alto, CA, seeks a regulatory affairs leader to own global strategy and execution for Portal's program, reporting to the Head of Regulatory Affairs. The role is strategic and hands-on, leading health authority interactions and acting as project manager for major submissions.

Required: NDA/BLA ownership, 5+ years in biotech/pharma regulatory affairs, strong cross-functional leadership, and ability to work in a fast-paced small company with global scope.

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Worksite address

palo alto, CA, 94306, US

Who can apply

Review the original listing for work authorization, qualifications and employer requirements.