Director, Regulatory CMC

Role: The position involves leading innovative biopharma projects within a unique funding model focused on rare diseases, emphasizing rapid development and scientific collaboration. Objectives include advancing early-stage research, defining ‘white space’ opportunities, and pushing therapeutic boundaries. Responsibilities encompass project leadership, cross-functional collaboration, supporting scientific and regulatory strategy, and fostering an environment of curiosity and innovation. The role emphasizes experimentation and ethical AI utilization. Qualifications: Bachelor's degree in relevant sciences, with significant experience in biopharma research or development (specific years not stated). Skills include strategic thinking, project management, and scientific expertise, particularly in rare diseases or novel modalities. The candidate should demonstrate a creative, boundary-pushing mindset and familiarity with early-stage clinical or preclinical research. High-Value: Focus on rare disease therapeutics, early-stage development, scientific innovation, and ethical AI use. The role supports a collaborative, fast-paced environment with a mission-driven culture. Work setup details and travel expectations are not specified, but the environment promotes teamwork and innovation.