
201 - 500 funcionários
Fundada em 2017
🧬 Biotecnologia
💊 Farmacêutico
🏥 Saúde
💰 $125.000.000 Post-IPO Equity - Stoke Therapeutics em 2024-03
Biotechnology • Pharmaceuticals • Healthcare
A Stoke Therapeutics é uma empresa de biotecnologia que desenvolve terapias baseadas em RNA para aumentar a produção de proteínas a partir dos genes do próprio paciente, visando o tratamento de doenças genéticas raras. Sua plataforma TANGO (Aumento Direcionado da Produção de Genes Nucleares) utiliza oligonucleotídeos antisense para aumentar a expressão gênica em distúrbios de haploinsuficiência. Os principais programas incluem o STK‑001, uma terapia antisense em desenvolvimento para a síndrome de Dravet (haploinsuficiência do SCN1A), além de outros programas focados em neurologia genética e indicações de doenças raras.
🕒 Julho 29
🗣️🇺🇸🇬🇧 Inglês obrigatório
Melhore suas chances de conseguir uma entrevista verificando sua pontuação de currículo antes de se candidatar.

201 - 500 funcionários
Fundada em 2017
🧬 Biotecnologia
💊 Farmacêutico
🏥 Saúde
💰 $125.000.000 Post-IPO Equity - Stoke Therapeutics em 2024-03
Biotechnology • Pharmaceuticals • Healthcare
A Stoke Therapeutics é uma empresa de biotecnologia que desenvolve terapias baseadas em RNA para aumentar a produção de proteínas a partir dos genes do próprio paciente, visando o tratamento de doenças genéticas raras. Sua plataforma TANGO (Aumento Direcionado da Produção de Genes Nucleares) utiliza oligonucleotídeos antisense para aumentar a expressão gênica em distúrbios de haploinsuficiência. Os principais programas incluem o STK‑001, uma terapia antisense em desenvolvimento para a síndrome de Dravet (haploinsuficiência do SCN1A), além de outros programas focados em neurologia genética e indicações de doenças raras.
• Develop and execute pre-launch and launch-phase access strategies, establishing Stoke’s presence with key accounts. • Serve as strategic leader for key accounts in the region. • Develop account-specific action plans that shorten the timeline from FDA approval to an active, positive coverage determination. • Build payer relationships and establish Stoke’s credibility with medical benefit policy decision-makers before NDA submission, ensuring seamless coverage between approval and patient access. • Develop multi-year access plans that anticipate commercial cycles and competitive coverage shifts, balancing account-level execution with a national access strategy. • Educate payers on clinical evidence, FDA labeling, treatment guidelines, and health-economic data to support coverage decisions and eliminate utilization management barriers (step edits, PA criteria, NDC blocks). • Monitor medical policy language at each account and partner with Medical Affairs, HEOR, and Advocacy to respond to and proactively shape policy criteria. • Proactively engage payer Medical Directors to obtain informal guidance letters or billing instructions that bridge the gap between launch and permanent J code assignment. • Engage and influence policy decision-makers for a medical benefit product to achieve desired coverage policy outcomes. • Serve as the company’s subject-matter expert on buy-and-bill reimbursement dynamics for products carrying a miscellaneous J code (J3490/J3590) pending assignment of a permanent, product-specific J code. • Educate payer medical policy teams on correct claims submission procedures, billing unit conventions, and NDC-to-J code crosswalk requirements to minimize claim denials during the unclassified code period. • Drive alignment across Stoke’s commercial team and field medical team without direct reporting relationships, building internal coalitions across Medical, HEOR, Reimbursement, Government Affairs, Legal, Trade & Distribution, and Patient Services to ensure integrated execution. • Ensure effective communication and coordination between the field reimbursement team and patient services to support a high approval success rate and timely patient access. • Engage authentically with the Dravet syndrome patient and caregiver community and incorporate community insights into payer engagement in a compelling and compliant manner. • Conduct all payer engagements in full compliance with company SOPs, OIG guidelines, PhRMA Code, and applicable federal and state regulations. • Navigate the unique complexity of a first-in-class disease-modifying ASO therapy with no established coverage precedent, finding creative and compliant paths to access.
• Bachelor's degree required; advanced degree (MBA, MPH, PharmD) preferred. • 15+ years in pharma/biotech; minimum 10 years in payer account management with lead responsibility for one of the three large PBM and National accounts. • Proven track record of achieving positive coverage outcomes for orphan designation or rare disease products on the medical benefit. • Pre-launch payer strategy experience—not just maintenance of established access. • Hands-on experience navigating a miscellaneous J code (J3490/J3590) environment, including transition to a permanent product-specific code. • Strong command of managed care economics, formulary management, utilization management, and coverage policy development processes at national payers. • Rare pediatric or neurological disease product launch experience; CNS or epilepsy payer experience a significant differentiator. • Familiarity with disease-modifying therapy and gene testing reimbursement pathways as established according to payer policy. • Experience at a company building its commercial infrastructure for the first time—startup or early commercial-stage biotech. • Exceptional ability to influence across functions without direct authority. • Passion for patient access and rare-disease impact.
• medical, dental and vision insurance • life, long- and short-term disability insurance • paid parental leave • a 401K plan with company match • unlimited vacation time • tuition assistance • participation in our Employee Stock Purchase Program (ESPP)
Candidatar-se🕒 Julho 29
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