Associate Director, Regulatory Affairs ROW | Hybrid

A leading biotechnology company in Princeton is seeking an Associate Director, Regulatory Affairs ROW to execute global regulatory strategies and manage compliance efforts. This role requires a PharmD, PhD, or MD with substantial experience in regulatory drug development. Key responsibilities include designing regulatory strategies and supporting marketing application submissions. The position operates on a hybrid model, requiring work in the office three days a week. Competitive salary and benefit packages are offered.
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