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 documents and ensures scientific integrity across all deliverables. 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 Rare Disease experience preffered, but ex...