Associate Director, Global Medical & Promotional Regulatory Affairs

Role: Associate Director, Global Medical and Promotional Regulatory Affairs at Jazz Pharmaceuticals, overseeing US promotional material review to ensure FDA compliance and support product launches. Responsibilities include leading the Promotional Material Review Committee (PMRC), providing regulatory guidance for advertising and promotional activities for oncology or neuroscience therapeutics, and managing interactions with FDA/OPDP. The role involves collaborating with Regulatory, Medical, Legal, Compliance, and Commercial teams to develop compliant promotional strategies, reviewing submissions, and maintaining current FDA regulatory knowledge. Qualifications: B.S./B.A. in a scientific discipline with significant pharmaceutical industry experience; direct experience in regulatory or promotional material review; strong understanding of FDA regulations; excellent judgment and communication skills. Preferred: advanced degrees (e.g., PharmD), industry-specific regulatory expertise. High-Value Details: Focus on pharmaceuticals in oncology and neuroscience, supporting product launches and promotional approvals, involving FDA interactions, with a senior level of responsibility. Work setup: US-based, with a salary range of $160,000-$240,000; some benefits and bonus eligibility.