
Global Regulatory Lead, Oncology – Strategy & Submissions
Vivid Resourcing, Boston, MA, United States
A clinical-stage biopharmaceutical company is seeking a Senior Director of Regulatory Affairs to lead global regulatory strategy for oncology programs. This role will drive regulatory pathways and interactions with health authorities, ensure compliance throughout development, and mentor staff. The ideal candidate will have over 12 years of experience within biotech, a strong background in oncology, and a proven track record with FDA submissions. This is a high-impact position offering visibility and career progression within the biotech sector.
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