Director, RA Global Regulatory Strategy

Role: Lead global regulatory strategy as Director Regulatory Affairs (GRL II) for AbbVie's therapeutic areas, including immunology, oncology, and neuroscience. Objectives: develop and execute strategies to secure and maintain product approvals, manage lifecycle regulatory activities, and ensure compliance with global requirements. Responsibilities: lead cross-functional Regulatory Product Teams, develop creative global regulatory strategies, oversee dossier content, and mitigate regulatory risks; serve as primary interface with regulatory agencies and internal stakeholders; guide regulatory policy and influence legislation; mentor team members and participate in industry initiatives. Qualifications: Bachelor's degree in life sciences; 7+ years of regulatory experience in pharma, with at least 5 years in strategic leadership; experience in drug development within US & EU regions, with a strong foundation in global regulatory strategies; advanced degree and certifications preferred. HighValue: extensive experience in pharmaceutical regulatory affairs, global drug development, especially in immunology, oncology, or neuroscience; managing compounds through all development stages and post-approval; impactful stakeholder engagement at senior levels; regulatory policy influence; working in complex, matrix environments. WorkSetup: location not specified; role involves leadership, strategic planning, and cross-functional collaboration across geographies.