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!