The Senior Director leads the delivery of high-priority AI and operational transformation initiatives by orchestrating cross-functional teams and aligning business needs with IT capabilities. They are responsible for end-to-end program governance, ensuring compliance with regulatory standards, and driving organizational adoption of AI-enabled workflows.
The Director leads the redesign of drug-development lifecycle workflows by identifying and embedding AI and automation solutions. They act as a bridge between business needs and IT, ensuring that all processes are scalable, compliant, and effectively adopted across the organization.
The Associate Director will write and coordinate clinical and regulatory documents such as protocols, investigator brochures, and clinical study reports. They will lead cross-functional teams to ensure high-quality, timely document delivery in compliance with regulatory guidelines.
The role involves managing a territory to drive patient diagnosis and care through HCP education and the promotion of approved products. The individual will develop strategic business plans and nurture relationships with key stakeholders including HCPs, genetic counselors, and pharmacists.
The Executive Director leads global Pharmacovigilance operations, ensuring compliance, inspection readiness, and strategic alignment with company growth. This role oversees case processing, vendor governance, quality systems, and regulatory reporting across the product lifecycle.
The Director provides strategic compensation counsel and leads global market intelligence, job architecture, and salary structure frameworks. They advise senior leadership on complex compensation solutions while ensuring alignment with global business strategies and pay equity standards.
The Senior Director serves as the medical lead for LC-FAOD and MPS franchises, overseeing regional medical strategy and US tactical launch plans. They are responsible for building key opinion leader relationships, leading data generation activities, and ensuring scientific accuracy across promotional and educational materials.
The Senior Medical Science Manager is responsible for building scientific relationships with key opinion leaders and medical organizations to enhance disease awareness and patient identification. They also provide clinical and scientific support to the company while contributing to local market access and clinical development strategies.
The Director of Regulatory Affairs Ad/Promo serves as a subject matter expert for the regulatory review of advertising and promotional materials in the U.S. and Canada. They lead the Materials Review Committee and act as the primary regulatory contact for agencies like the FDA and PAAB.
The Senior Medical Science Liaison will serve as a key link between the company and the rare disease medical community, delivering critical scientific information regarding the metabolism portfolio. They will also develop engagement plans for key opinion leaders and support clinical research initiatives to enhance patient outcomes.
The Regional Director will lead a team of UltraCare Liaisons to drive the commercialization and growth of the neurology portfolio. They are responsible for strategic business planning, team development, and fostering relationships with key stakeholders in the rare disease community.
The Regional Director will lead a team of UltraCare Liaisons to drive the commercialization and growth of the neurology portfolio within a specific region. This role involves strategic planning, team coaching, and cross-functional collaboration to ensure patient access and business performance.
The Regional Director will lead a team of UltraCare Liaisons to drive the successful launch and commercial growth of the neurology portfolio. This role involves strategic planning, coaching, and fostering cross-functional partnerships to ensure patient access and market adoption.
The Regional Director will lead a team of UltraCare Liaisons to drive the commercial launch and growth of the neurology portfolio. They are responsible for strategic planning, coaching, and fostering cross-functional collaboration to ensure patient access and business performance.
The Director of US Marketing will lead the development and execution of marketing initiatives for the commercialization of Dojolvi and Mepsevii. This role involves cross-functional collaboration to drive brand strategy, market conditioning, and patient access while mentoring the marketing team.
Develop and execute the Japan Medical Plan and local medical strategies to enhance relationships with medical thought leaders. Support clinical trial operations in Japan and provide scientific support for product development and commercialized brands.
