Senior Medical Writer, Regulatory & Publications Lead

A biotechnology company in Boston is seeking a Senior Medical Writer to produce and manage clinical and regulatory documents for up to 5 clinical studies. The candidate should possess extensive industry experience, preferably with NDA/BLA submissions. Responsibilities include writing protocols, managing review processes, and providing training in writing practices. Ideal applicants need a bachelor's or advanced degree in life sciences and strong communication skills. This strategic role is crucial to the clinical operations team's success.
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