Clinical Development Executive Medical Director

Role: Clinical Development Executive Medical Director specializing in GU therapeutics, focusing on Enfortumab vedotin. Main objectives include defining and executing clinical development strategies, overseeing trial design and delivery, and integrating regulatory and stakeholder input. Responsibilities encompass leading global development teams, managing clinical protocols, interpreting data, and contributing to regulatory submissions and meetings. Requirements: Medical degree or equivalent with 4+ years industry experience, 7+ years in clinical development, and 5+ years leading teams; board certification in oncology preferred. High-value specifics: oncology, bladder cancer, biologics (antibody-drug conjugate), clinical phases (likely early to late-stage trials), regulatory submissions (NDA, BLA, MAA). The role involves global travel, with flexibility for non-standard hours, and reports to the Therapeutic Area Head. May have management responsibilities for up to 6 medical professionals. Work setup: hybrid; occasional travel required.