Director, Medical Writing

August 25

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Nuvalent, Inc.

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Description

• Reporting to the VP, Clinical Development, the Director, Medical Writing will provide leadership to the medical writing function and oversee medical writing projects across Nuvalent’s growing clinical pipeline. • The individual will be responsible for strengthening Nuvalent’s medical writing capabilities, efficiency and quality, as well as recruiting and managing medical writing resources. • Provide leadership, strategic direction and hands-on oversight for the medical writing function, including resource allocation, process, quality, and timelines. • Recruit, train, develop, and allocate medical writing resources, including outsourcing where necessary. • Proactively identify process improvements to enhance medical writing efficiencies, capabilities, and quality. • Plan, coordinate, critically review and/or author medical writing deliverables.

Requirements

• 10 years of relevant medical writing experience within the pharmaceutical industry. • In-depth understanding and familiarity with regulatory standards and best practices relating to development of clinical/regulatory documents. • Experience managing in-house and external medical writers. • Experience developing and optimizing medical writing processes. • Oncology experience is strongly preferred. • Prior experience in development of New Drug Application/MAA is strongly preferred.