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Senior Principal Medical Writer: Regulatory Lead

The Steely Group

The Steely Group seeks a Senior Principal Medical Writer to independently write and manage complex clinical documents including protocols, master plans, and study reports. You will lead cross-functional teams and oversee IND/CTA/ NDA/MAA submissions while mentoring contractors and junior writers.

Applicants should have an advanced degree and 10+ years of regulated life sciences writing experience, with strong expertise in global submissions and eCTD tools.

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Vacancy posted 2 days ago
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