Simon-Kucher
Market Access Manager – Pharma & AMNOG (m/w/x)
Vollzeitmit HomeofficeBerufserfahren
Berlin, Bonn, Köln, Frankfurt am Main, Hamburg, München
BRBridgeBio Pharma
Market Access Manager, EU Center (m/w/x)
Vollzeitmit HomeofficeSenior
Nejo KI-Zusammenfassung
Securing patient access to medicines across DACH, owning the German AMNOG process end-to-end. Deep AMNOG and HTA expertise required. Performance-based financial rewards, growth opportunities.
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Anforderungen
- Deep AMNOG and HTA expertise
- Strong communication skills
- Adaptability
- Ability to thrive in fast-paced environment
- Ability to thrive in hands-on environment
- Degree in health economics, pharmacy, medicine, life sciences or comparable field
- Experience preparing AMNOG value dossiers under § 35a SGB V
- Project lead on at least one complete AMNOG procedure
- Hands-on involvement in reimbursement price negotiation under § 130b SGB V
- Solid command of G-BA methodology
- Solid command of IQWiG methodology
- Solid command of G-BA procedural rules
- Solid command of IQWiG procedural rules
- Solid command of G-BA statutory timelines
- Solid command of IQWiG statutory timelines
- Ability to appraise clinical evidence critically
- Ability to translate clinical evidence into payer-ready argumentation
- Experience engaging payers directly on reimbursement matters
- Experience engaging hospitals directly on reimbursement matters
- Confidence to lead payer conversations
- Confidence to lead hospital conversations
- Knowledge of German hospital financing (NUB, DRG, additional payments)
- Knowledge of reimbursement in Austria
- Knowledge of reimbursement in Switzerland
- Strong written argumentation skills
- Ability to work autonomously in an environment with developing processes
- Experience with orphan drugs
- Experience with limited evidence base
Aufgaben
- Report to the Senior Director, Market Access, EU Center
- Collaborate with Medical Affairs, HEOR, Regulatory, Commercial, and global Market Access teams
- Secure and sustain patient access to medicines across the DACH region
- Own the German AMNOG process end to end
- Manage value dossier creation under § 35a SGB V
- Negotiate reimbursement prices with GKV-Spitzenverband under § 130b SGB V
- Engage with sickness funds, Medical Service, physicians’ associations, hospitals, and treating centers for regional market access
- Lead reimbursement submissions in Austria and Switzerland
- Collaborate with cross-functional colleagues and external stakeholders for high-quality execution
- Plan, resource, quality-assure, and submit AMNOG value dossiers under § 35a SGB V
- Derive appropriate comparator therapy (zVT)
- Identify evidence gaps and develop argumentation on indirect comparisons, surrogate, and subgroup analyses
- Prepare scientific advice requests under § 8 AM-NutzenV
- Manage G-BA and IQWiG interactions, including written commenting procedures and oral hearings
- Manage all procedural communication and timelines with G-BA and IQWiG
- Develop pricing strategy, negotiation mandate, scenarios, and European reference price analyses
- Plan for arbitration board risk
- Engage sickness funds at federal and regional levels on reimbursement, cost-efficiency reviews, and prior-authorisation practice
- Engage the Medical Service (MD) on reimbursement, cost-efficiency reviews, and prior-authorisation practice
- Engage regional physicians’ associations (KVen) on reimbursement, cost-efficiency reviews, and prior-authorisation practice
- Translate payer insights into regional access concepts
- Advise treating centers on NUB applications
- Advise treating centers on DRG and additional-payment (ZE) mapping
- Advise treating centers on budget and price negotiations
- Advise treating centers on drug committees and formulary listing
- Advise treating centers on outpatient care via ASV under § 116b SGB V
- Handle individual reimbursement requests, denials, and claw-backs
- Collaborate with Medical Affairs and field teams to resolve access barriers
- Develop argumentation aids and training material from recurring issues
- Lead reimbursement submissions in Austria (EKO)
- Lead reimbursement submissions in Switzerland (FOPH Specialities List)
- Incorporate market access requirements into study design
- Incorporate market access requirements into evidence planning
- Incorporate market access requirements into launch planning
Berufserfahrung
5 - 8 Jahre
Ausbildung
Bachelor-Abschluss
Sprachen
Deutsch – verhandlungssicher
Englisch – verhandlungssicher
Benefits
Weiterbildungsangebote
- Career development programs
- Skill development opportunities
- Continuous education programs
- Professional development programs
Boni & Prämien
- Financial rewards for performance
- Referral bonus
Lockere Unternehmenskultur
- Peer-to-peer recognition
Karriere- und Weiterentwicklung
- Growth opportunities
- Internal mobility opportunities
- Career pathing
Betriebliche Altersvorsorge
- 401(k) with employer match
Attraktive Vergütung
- Employee Stock Purchase Program
Parkplatz & Pendelvorteile
- Pre-tax commuter benefits
- Subsidized parking
Gratis oder Vergünstigte Mahlzeiten
- Subsidized lunch
Gesundheits- & Fitnessangebote
- 100% employer-paid medical premiums
- 100% employer-paid dental premiums
- 100% employer-paid vision premiums
- Health Savings Account with employer contributions
Sonstige Zulagen
- Flexible Spending Accounts
Sonstige Vorteile
- Fertility benefits
- Comprehensive paid medical leave
Familienfreundlichkeit
- Family-forming benefits
Mentale Gesundheitsförderung
- Expanded mental health support
Flexibles Arbeiten
- Hybrid work model
- Flexible paid time off
Mehr Urlaubstage
- Company-paid holidays
Großzügige Elternzeit
- Comprehensive paid parental leave
Von Nejo automatisch aufbereitet
Nejo hat diesen Job automatisch von der Website des Unternehmens BridgeBio Pharma erfasst und die Informationen auf Nejo mit Hilfe von KI für dich aufbereitet. Trotz sorgfältiger Analyse können einzelne Informationen unvollständig oder ungenau sein. Bitte prüfe immer alle Angaben in der Originalanzeige! Inhalte und Urheberrechte der Originalanzeige liegen beim ausschreibenden Unternehmen.
Zur Originalanzeige bei BridgeBio PharmaÜber das Unternehmen
BR
PharmaceuticalsBerlin
BridgeBio is a biopharmaceutical company dedicated to discovering, developing, and delivering transformative medicines for patients living with genetic diseases and genetically defined cancers.
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