Associate Director, Global Regulatory Submissions

A biopharma company in Waltham, Massachusetts, is seeking an Associate Director of Regulatory Operations. This role is pivotal for managing regulatory submissions across the USA and EU, ensuring high-quality dossiers and compliance with global standards. The ideal candidate will have at least 8 years of experience in regulatory operations, with expertise in the eCTD submission process and tools like Docu Bridge and Veeva.

Competitive compensation and comprehensive benefits are offered, including a robust professional development program.
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