Senior Regulatory Writer, Clinical Submissions Lead

A global biopharmaceutical company in the United Kingdom is seeking a Senior Regulatory Writer to lead projects involving high-quality regulatory documentation. This role requires a Bachelor's degree and at least 3 years of experience in regulatory writing or clinical documentation. You will manage project teams, author documents according to regulatory authority guidelines, and provide mentorship to junior writers. If you're passionate about helping clients navigate the regulatory process, this opportunity is ideal for you.
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