Associate Director, Regulatory Affairs (Regulatory Intelligence)

Role: Associate Director, Regulatory Affairs (Regulatory Intelligence) at Telix Pharmaceuticals, focusing on monitoring and analyzing global regulatory developments to ensure compliance and strategic positioning for radiopharmaceutical products in oncology and rare diseases. Responsibilities include tracking regulatory changes from authorities like FDA and EMA, maintaining intelligence databases, providing insights to internal teams, and supporting regulatory strategy development. The role also involves leading cross-functional discussions, managing external stakeholder engagement, and driving continuous improvement of processes. It includes leadership responsibilities such as team oversight and professional development. Qualifications: Bachelor's in life sciences, law, or related field; 8+ years in pharmaceutical regulatory affairs with 6+ years in regulatory intelligence, familiarity with drug, biologic, and device regulations, and experience with agencies like FDA, EMA, or PMDA. Preferred: Master’s degree and prior interaction with health authorities. High-Value: Focus on pharma regulatory landscape, global scope, and strategic influence in oncology and rare disease markets. Work setup: Hybrid or remote, with a global team.