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 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!