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Ultragenyx Pharmaceutical, founded in 2010, is a biotechnology company that specializes in bringing products to market to treat rare, ultra-rare, and serious genetic diseases and c
Global Medical Director LC FAOD and MPS
Location
United States
Posted
98 days ago
Salary
$259.6K - $320.7K / year
Seniority
Lead
No structured requirement data.
Job Description
Global Medical Director LC FAOD and MPS
Ultragenyx Pharmaceutical
This description is a summary of our understanding of the job description. Click on 'Apply' button to find out more. Role Description Ultragenyx is seeking an experienced physician leader with a passion for rare and ultra-rare diseases. Reporting to the Global Medical Lead, the Director will be a key contributor to shaping the strategy and executing the medical affairs plans for LC-FAOD, MPS VII, and MPS IIIA. This role offers a unique opportunity to be part of highly collaborative cross-functional teams working on both approved therapies (Dojolvi and Mepsevii) and an investigational AAV gene therapy (UX111) as we prepare for future potential launches. 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: - Provide strategic medical and scientific leadership to LC‑FAOD (Dojolvi) and the MPS programs (MPS VII and MPS IIIA) to support the development and execution of the global medical plans. - Contribute to the development and execution of the annual Integrated Evidence Generation Plans. - Provide medical expertise and leadership to Real-World Evidence initiatives (e.g., ISTs, collaborative research) and the Disease Monitoring Programs for LC‑FAOD and MPS focused on data generation and publication activities. - Act as a subject matter expert in assigned therapeutic areas, guiding and contributing to the execution of key global medical affairs activities including advisory boards, medical education initiatives, and congress activities. - Lead robust scientific engagement and education, maintaining strong relationships with external stakeholders to generate insights and advance scientific understanding of assigned programs. - Provide scientific and medical leadership as needed for publication and medical communication material development. - Serve as a medical reviewer for promotional materials and non-promotional scientific materials ensuring accuracy, balance, strategic alignment, and compliance with regulatory requirements. - Provide subject matter expertise to develop and deliver training across the organization. - Collaborate cross-functionally with Clinical Development, Commercial, Regulatory, HEOR, Biostatistics, Patient Advocacy, Regional Medical Teams, and others to achieve program goals. Qualifications - Medical Doctor (MD or DO) required. - Clinical expertise in the management of patients with inherited metabolic and/or neurodegenerative rare diseases strongly preferred. - At least 2 years of experience in the pharmaceutical industry is preferred, but extensive relevant clinical experience may be considered as an alternative. - Strategic thinker with strong execution discipline and a proven ability to manage multiple projects. - Ability to interpret and communicate complex clinical and scientific information to a range of audiences. - Highly analytical in approach to work, with the ability to identify interdependencies, consider the medical implications, and understand the broader goals of a program and the organization. - Ability to work independently and as a member of a cross-functional matrix team in a fast-paced environment. - High attention to detail, demand for high-quality work, and sense of passion and urgency to achieve goals and improve the lives of patients. - Willingness and ability to travel up to 15%, including domestic and international engagements. Benefits - Generous vacation time and public holidays observed by the company. - Volunteer days. - Long term incentive and Employee stock purchase plans or equivalent offerings. - Employee wellbeing benefits. - Fitness reimbursement. - Tuition sponsoring. - Professional development plans. - Benefits vary by region and country.
Job Requirements
- Medical Doctor (MD or DO) required.
- Clinical expertise in the management of patients with inherited metabolic and/or neurodegenerative rare diseases strongly preferred.
- At least 2 years of experience in the pharmaceutical industry is preferred, but extensive relevant clinical experience may be considered as an alternative.
- Strategic thinker with strong execution discipline and a proven ability to manage multiple projects.
- Ability to interpret and communicate complex clinical and scientific information to a range of audiences.
- Highly analytical in approach to work, with the ability to identify interdependencies, consider the medical implications, and understand the broader goals of a program and the organization.
- Ability to work independently and as a member of a cross-functional matrix team in a fast-paced environment.
- High attention to detail, demand for high-quality work, and sense of passion and urgency to achieve goals and improve the lives of patients.
- Willingness and ability to travel up to 15%, including domestic and international engagements.
Benefits
- Generous vacation time and public holidays observed by the company.
- Volunteer days.
- Long term incentive and Employee stock purchase plans or equivalent offerings.
- Employee wellbeing benefits.
- Fitness reimbursement.
- Tuition sponsoring.
- Professional development plans.
- Benefits vary by region and country.
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