Senior Director, Clinical Development

Role: Senior Director, Clinical Development responsible for supporting in-licensing, acquisitions, and cross-functional research alignment in immunological disorders. Responsibilities: provide clinical evaluation for external molecule assessments, contribute to clinical development planning for assets from Late Lead Optimization, support transition teams for in-licensed or acquired assets, monitor science and standards, and collaborate on clinical study designs and safety management. Requirements: MD or MD/PhD with board certification in internal medicine (e.g., Rheumatology, Transplantation), 7+ years of clinical development experience across modalities including small molecules and biologics, familiarity with regulatory pathways (FDA, EMA, PMDA), experience in global Phase 1–2a programs, and ability to influence cross-functional teams. Preferred: experience with combination drug-device development, NDA/MAA submissions, and late-stage development. High-Value: focus on immunological disorders, early clinical phases, global regulatory expertise, and remote work with occasional travel (~10%). Collaboration with external medical experts and internal discovery teams is integral. Work setup: fully remote, with occasional domestic/international travel.