Editas Medicine is seeking a Vice President, Regulatory Affairs to lead the global regulatory function for in vivo gene editing therapies. You will implement strategy, manage submissions, and act as the primary regulatory advisor to executives and partners.
Reporting to the Chief Medical Officer, you will oversee interactions with health authorities, steer evidence-generation plans, and drive regulatory readiness across development programs in a lean organization.
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📌 Head of Regulatory Affairs, Gene Editing (Town of Cambridge)
🏢 Editas Medicine
📍 Town of Cambridge
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