Provide leadership for the integration of scientific information activities across core program teams.
Ensure continuity and consistency of scientific data interpretation and messaging across development and commercialization stages.
Oversee the development and execution of integrated, lifecycle-based publication strategies.
Ensure publications support launch readiness, scientific leadership, and long-term evidence generation.
Provide strategic oversight for clinical trial disclosure and data sharing activities.
Partner with Medical Affairs leadership on evidence planning, scientific platforms, and content optimization.
Lead the identification, evaluation, and implementation of AI-enabled and digital tools for scientific workflows.
Collaborate with stakeholders in Clinical Development, Regulatory Affairs, Commercial, and Medical Affairs.
Cross-functional Team LeadershipStakeholder management
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About Ultragenyx Pharmaceutical
Ultragenyx pioneers life-changing treatments for rare genetic diseases. You will help patients who often have no other options. We develop novel therapies across bone, endocrine, metabolic, muscle, and CNS categories. Our portfolio includes FDA-approved products like Crysvita, Mepsevii, and Dojolvi. These medicines serve patients globally, including Canada, Europe, Latin America, and Japan. With over $1.1 billion in funding across six rounds, we continue to expand our reach and impact. You contribute to a company actively transforming patient lives through scientific innovation and a commitment to unmet medical needs.
How We Work
Ultragenyx embraces a remote-first philosophy for many roles. Our team members work full-time from home, traveling to offices or other locations as needed. This model supports flexibility while fostering collaboration. We believe in creating a supportive, inclusive environment for learning and growth. Our culture focuses intensely on patient needs, guiding every decision and action. You will find a workplace recognized by BioSpace as a best company, where your contributions make a tangible difference.
Why Join Us
Drive meaningful impact for patients with rare genetic diseases.
Contribute to a company with $1.1B in funding and a robust product pipeline.
Work in a remote-friendly environment that prioritizes flexibility and employee well-being.
Benefit from generous vacation, employee stock plans, and professional development resources.
Shape the future of rare disease medicine in a recognized 'best place to work' culture.
Benefits & Perks
Generous vacation time and observed public holidays
Volunteer days
Long term incentive and Employee stock purchase plans