Regulatory Medical Writing Lead - Hybrid, Program Impact

A multinational pharmaceutical company is seeking an Associate Director of Regulatory Medical Writing in Raritan, NJ. This hybrid role involves leading writing teams for clinical submissions, managing direct reports, and ensuring high-quality standards in documentation. Candidates should possess significant experience in medical writing, project management, and leadership. The position offers robust benefits, a salary range of $137,000 to $235,750, and opportunities for professional development in a dynamic work environment. J-18808-Ljbffr