Lead the development, optimization and continuous improvement of Regulatory Intelligence tools and processes, Proactively monitor, assess and interpret emerging global regulatory developments, guidelines, and relevant competitive intelligence, Translate Regulatory Intelligence information into clear, actionable insights that support our regulatory strategy and cross-functional decision-making, Drive the review, synthesis and dissemination of regulatory intelligence within Regulatory Affairs and to relevant stakeholders, Oversee and coordinate the structured documentation, tracking and maintenance of Regulatory Intelligence information within internal systems, Provide regulatory support for Immatics development programs, including preparation, review and contribution to documentation for CTA applications and subsequent modifications, with a focus on clinical and/ or CMC aspects, Help ensure that regulatory documentation meets applicable requirements, guidelines, and quality standards