Contribute to the implementation of the global development strategy, leading or co-leading clinical trials in various stages of development, and overseeing all aspects of clinical development working closely with the Medical Director and cross-functional teams to ensure high-quality, timely deliverables. Collaborate with the Medical Director to develop clinical and regulatory documents, including safety updates, registration dossiers, protocols, ICFs, IBs, study reports, and regulatory submissions to support registration and commercialization.