Director, Medical Information
UltragenyxAbout the role
Position Summary:
ultrafocused – Work together to fearlessly uncover new possibilities
The Director, Head of Global Medical Information is responsible for setting the strategic direction, operational excellence, and scientific rigor of Ultragenyx’s global medical information function. This leader ensures the accurate, balanced, and timely communication of scientific information to healthcare professionals, patients, and internal stakeholders across Ultragenyx’s rare disease portfolio.
Reporting to the Head of Scientific Communications, the Director oversees both internal team members and external vendor partners, while contributing directly to the development and review of scientific materials. This “player–coach” role is critical to ensuring inspection ready medical information operations, compliant scientific exchange, and seamless alignment with Medical Affairs, Regulatory, Pharmacovigilance, Legal, and Commercial partners.
Work Model:
Remote: Officially documented as working full-time from home, with travel to Ultragenyx's offices or other locations on occasion as needed.
Responsibilities:
Global Medical Information Leadership
- Lead the global medical information strategy and operations, ensuring compliant, evidence based responses to unsolicited inquiries from HCPs, patients, and internal teams.
- Oversee creation, review, and maintenance of global standard response letters, FAQs, and medical information resources across marketed and pipeline programs.
- Ensure all materials remain scientifically current, aligned with evolving data, and consistent with regulatory expectations globally.
Inquiry Management & Vendor Oversight
- Provide strategic direction and quality oversight for outsourced medical information contact center operations.
- Define performance standards, service metrics, and quality management processes for vendor partners.
- Ensure clear triage pathways and timely escalation of complex scientific inquiries to internal experts.
- Monitor inquiry trends to identify emerging knowledge gaps, safety issues, or reputational risks.
- Maintain inspection readiness for all medical information systems, processes, and documentation.
Medical Review & Scientific Governance
- Serve as Medical reviewer within the Medical–Legal–Regulatory process for assigned assets.
- Provide scientific review of medical information materials, HCP resources, training content, and other scientific communications.
- Ensure all externally facing materials are accurate, balanced, and aligned with current evidence and regulatory guidance.
- Guide the appropriate handling of off label and unsolicited scientific inquiries.
Scientific Content Strategy
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