Global Regulatory Affairs Lead - IND/CTA Submissions

A biopharmaceutical company in South San Francisco is seeking an Associate Director of Regulatory Affairs to lead global regulatory activities for clinical-stage programs. Responsibilities include preparing regulatory submissions, interacting with health authorities, and contributing to regulatory strategies. The ideal candidate will have over 7 years of experience in regulatory affairs, a strong understanding of ICH guidelines, and proven skills in project management. Competitive salary range is $197,000-240,000 with bonuses and robust benefits.
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