
Associate Director, US Patient Advocacy
Posted 2 days ago

Posted 2 days ago
This is a fully remote position, open to applicants in United States.
• Develop and implement strategies and engagement plans for patient advocacy across various disease therapeutic areas in alignment with corporate goals.
• Balance and prioritize both pipeline and in-market indications, including gMG and CIDP.
• Execute patient advocacy engagement strategies at both national and local levels in collaboration with cross-functional teams.
• Translate US and market strategies into practical tactics and events.
• Establish and manage relationships with US Patient Advocacy Organizations.
• Gain insights into patient needs through events, panels, and other engagement opportunities.
• Provide localized support to the patient services team during the onboarding process for patients.
• Represent argenx at external events and conferences to educate and engage with patients.
• Define and assess the business impact at local, regional, and national events.
• Maintain a thorough understanding of disease states, Patient Experience, and product knowledge.
• Generate and synthesize insights to guide local market engagement.
• Collaborate across functions to identify patient advocacy needs and opportunities.
• Advocate for the patient community within argenx and the Advocacy team.
• Manage compliant events, sponsorships with patient advocacy organizations, and budgetary considerations.
• Oversee the Advocacy strategy for assigned indications from development to market launch in partnership with TA-level Advocacy colleagues.
• Ensure alignment and prioritization of activities through established frameworks, standardization, and effective ways of working.
• Travel meaningfully within designated geographies and attend prioritized patient events, whether in-person or virtually.
• A Bachelor’s Degree is required.
• A minimum of 10 years of experience in the industry or a related field.
• Demonstrated ability and success in implementing innovative programs within rare diseases and among minority and underserved patient populations.
• A proven track record of establishing and adhering to an Advocacy strategy for a specific indication or Therapeutic Area.
• Proficiency in Veeva is required.
• Experience with patient interactions in the rare disease sector and compliance is mandatory.
• Willingness to travel up to 50% of the time is essential.
• Availability to attend events outside of standard business hours, including weekends and evenings.
• An advanced degree is preferred.
• Short-term and long-term incentive programs, in accordance with applicable plans and policies.
• A comprehensive benefits package.
• Retirement savings plans.
• Health benefits.
• Additional benefits as per applicable plan and program guidelines.
• Flexible schedule to accommodate work during evenings and weekends.
• An inclusive environment that ensures equal consideration without discrimination.
• Reasonable accommodations available during the application process, interviews, or candidate selection activities.
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