• Lead and demonstrate ownership of the design and implementation of a clinical development program • Oversee project-related education of investigators, study site personnel, and study staff • Responsible for leading clinical study teams and monitoring overall study integrity • Present at scientific, medical, and regulatory meetings globally • Develop and maintain relationships with academic investigators, pharmaceutical partners/sponsors, and patient advocacy groups • Contribute to company’s planned regulatory filings including authoring clinical sections for INDs, NDAs, and related documents