ARTO is currently partnered with a globally renowned mid sized Pharmaceutical company who are committed to the development of drugs within the Rare Disease space. With a growing clinical development team, we are currently searching for a Medical Director in their Clinical Development group who will be able to assist with the development of drugs from proof of concept up to the crucial NDA/BLA submission phase. Key Responsibilities: Medical Oversight : Acts as Medical Monitor, overseeing study execution, subject eligibility, and safety surveillance. Scientific Leadership : Provides medical input on clinical study and protocol design, as well as driving clincial and project groups through execution Data Analysis & Interpretation : Critically evaluates study data and contributes to the integration and interpretation of results. Strategic Contribution : Supports the Clinical Development Plan (CDP) by aligning studies with broader clinical and scientific strategy. Stakeholder Collaboration : Engages with internal teams and external physician stakeholders to inform clinical decisions and ensure relevance. Experience Needed: MD/MD PhD 5 Years experience in the pharmaceutical industry Experience as a Clinical Lead Rare Disease experience preffered, but experience developing drugs in the wider Immunology space is also acceptable If you'd like to hear more, please reach out to me on jamie.stephens@arto-talent.com, or directly on LinkedIn DM!