Director, Clinical Development Sciences

Role: Lead clinical development sciences for global rare disease programs, ensuring high-quality data collection, analysis, and regulatory compliance across all study phases. Responsibilities: oversee program design, protocol review, trial execution, and data interpretation; contribute to regulatory submissions and scientific documentation; serve as SME for clinical strategies and regulatory questions; lead multidisciplinary teams, including study scientists and cross-functional partners; support external dissemination of trial data and interactions with investigators and regulators; manage and mentor staff, setting goals and training. Requirements: bachelor’s degree (advanced degree such as MD/PhD/PharmD strongly preferred); 10+ years in pharmaceutical development with at least 3 years in a sponsor role; extensive experience in clinical trial design, data interpretation, GCP, and global regulatory processes; proven leadership in cross-functional teams; experience in rare diseases desirable. HighValue: rare disease (hereditary angioedema), clinical development, global regulatory interactions, protocol design, study oversight, cross-disciplinary leadership, ≥10 years industry experience. WorkSetup: not specified; likely hybrid or onsite given role scope.