Regulatory Affairs Leader, Global Submissions & Strategy

A clinical-stage biopharmaceutical company is seeking an Associate Director, Regulatory Affairs to lead regulatory strategy and submissions for clinical programs. This role involves collaborating with cross-functional teams, conducting regulatory research, and managing submissions to ensure compliance with regulatory standards. Candidates should have 7+ years of experience in regulatory affairs, a strong understanding of ICH guidelines, and excellent communication skills. This position offers a competitive salary and robust benefits, emphasizing the company's commitment to innovation in healthcare.
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