National Outcomes Director – Payer, VIASKIN® Peanut East

🕒 il y a 2 mois

🏖️ New Jersey – Distant

🏖️ New Jersey – Remote

💵 $200 000 - $240 000 / an

⏰ Temps Plein

🔴 Expert

👔 Directeur

👻 Score fantôme 17%

Ce que ça veut dire : la probabilité que cette offre reste ouverte sans recrutement actif.Comment le lire : 60 % ou plus, on pense que c'est une offre fantôme. Un score plus bas est moins inquiétant.Comment on la calcule : ancienneté, republications, postes ouverts vs taille de l'équipe, rapidité de clôture, et si le salaire est indiqué.À noter : une estimation à partir de données publiques, pas un jugement sur l'entreprise. De vraies offres peuvent avoir un score élevé, alors prenez-le comme un indice, pas comme un fait.

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DBV Technologies

Site WebLinkedInTous les Emplois

51 - 200 employés

🏥 Santé

🍽️ Alimentation et boissons

🧬 Biotechnologie

🔥 Financement dans la dernière année

💰 €30 000 000 Post-IPO Secondary - DBV Technologies en 2025-10

Healthcare • Food & Beverage • Biotechnology

DBV Technologies est une société biopharmaceutique mondiale en phase clinique, développant une immunothérapie épicutanée pour traiter les allergies alimentaires et d'autres maladies à médiation immunitaire. Fondée par des pédiatres, l'entreprise fait progresser sa technologie brevetée de patch VIASKIN® à travers des essais cliniques, y compris des études de Phase 3 pour un patch contre l'allergie à l'arachide (DBV712) et des programmes en phase initiale pour l'allergie au lait (DBV135), dans le but de rééduquer le système immunitaire en utilisant une exposition contrôlée de la peau à des antigènes.

Description

• Serve as a scientific expert and key point of contact between DBV Technologies and external payer and population health decision-makers • Communicate evidence-based information on VIASKIN Peanut’s value proposition and pediatric food allergy health outcomes • Engage national and regional payers, PBMs, IDNs, employers, and population health key opinion leaders • Communicate efficacy, safety, patch wear-time, and real-world relevance to support coverage and formulary decisions • Conduct educational programs, scientific presentations, and value-evidence discussions • Establish and maintain relationships with medical and pharmacy directors, payer decision-makers, professional societies, and patient advocacy organizations • Disseminate health outcomes data, real-world evidence, health economic models, and budget-impact analyses • Collaborate with Market Access, Medical Affairs, Value & Access, Commercial, and Field Reimbursement teams • Design outcomes-based analytics using internal data sources and external vendors such as IQVIA, Optum Insights, and Komodo • Train internal teams on outcomes data and value evidence • Address unsolicited payer inquiries in accordance with regulations and company policy • Support investigator-initiated studies, real-world evidence generation, and other research initiatives • Contribute to strategic plans for health outcomes research, value-evidence communication, and payer engagement • Integrate health outcomes strategies into product launch, access, and commercialization plans • Ensure communications and interactions comply with regulatory requirements, legal guidance, and company policies

🎯 Exigences

• PharmD, M.D., or Ph.D. in a health sciences–related field required • Master’s in pharmacoepidemiology, epidemiology, or health economics preferred • Minimum of eight (8) years working in the pharmaceutical, biotechnology, or healthcare industry • Minimum of five (5) years in a HEOR or payer-facing scientific function supporting product launches with U.S. Market Access teams • Experience spanning medical and scientific affairs, outcomes research, clinical practice, academic, or U.S. managed-markets settings • Therapeutic experience in allergy/immunology, pediatrics, and/or rare disease preferred; familiarity with the food allergy treatment landscape is a strong advantage • Strong understanding of health outcomes research, epidemiology, and health economics • Demonstrated experience engaging national and regional payers, PBMs, IDNs, and other organized customers in a scientific or value-evidence capacity • Expertise in economic modeling, budget-impact analysis, data analysis, and interpreting clinical and real-world data • Knowledge of industry trends, healthcare policies, and regulations impacting HEOR • Understanding of therapeutic areas, disease mechanisms, treatment landscapes, and market dynamics • Excellent written, verbal, communication, and presentation skills • Strong proficiency with regulatory guidelines and requirements related to HEOR studies and payer scientific exchange • Understanding of compliance and ethical considerations in research and payer engagement • Ability to build relationships with external stakeholders, thought leaders, and academic HEOR experts • Ability to collaborate cross-functionally, manage multiple projects, prioritize tasks, meet deadlines, and adapt to changing priorities • Proficiency in resource allocation, budget management, and project planning • Comfort operating in an ambiguous, fast-paced, pre-commercial environment • Ability to articulate clearly and conduct presentations with large and small audiences