Global Regulatory Affairs Director (Neuroscience)

About this role

Requirements

• Degree in a science‑based discipline (BSc or MSc).
• Demonstrated experience in global regulatory affairs and pharmaceutical development, spanning early‑ to late‑stage programmes.
• Proven capability in leading complex global regulatory strategies, ideally within Neuroscience and innovative or rare disease areas.
• Strong experience with major global submissions, including registration, accelerated pathways, and significant lifecycle variations.
• Deep understanding of Health Authority engagement, regulatory guidance interpretation, and strategic negotiations.
• Track record of operating as a core member of Global Program Teams, influencing development, approval, and lifecycle strategy.
• Excellent communication, influencing, and problem‑solving skills.
• Commitment to Diversity and Inclusion / EEO paragraph
• Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve.