Associate Director, Safety Analysis Scientist
This role involves leading scientific safety evaluations for pharmaceutical products across development and post-marketing stages, with a focus on analyzing complex medical data, shaping safety strategies, and supporting regulatory compliance. The scientist will serve as a subject matter expert, lead cross-functional safety reviews, contribute to key clinical documents, and drive innovation in safety analysis methodologies. Emphasis is placed on proactive risk assessment, collaboration with global teams, and ensuring high-quality, timely safety reporting.