Strategic Lead, Clinical Regulatory Writing

Zenith LifeScience in the United States is seeking a Clinical Regulatory Writing Associate Director to lead complex regulatory writing across drug development programs. You will oversee authoring of strategic regulatory documents and collaborate with cross-functional teams to ensure timely, compliant submissions.
The role requires extensive medical writing experience in pharma or CROs, strong leadership, and the ability to guide vendor writers and internal teams through MAA, IND, and NDA

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