Market Access Manager, EU Center

This is a fully remote position, open to applicants in Germany.

📋 Description

• Report directly to the Senior Director of Market Access for the EU Center.

• Work collaboratively with Medical Affairs, HEOR, Regulatory, Commercial, and the global Market Access team.

• Ensure and maintain patient access to BridgeBio’s medications throughout the DACH region.

• Manage the German AMNOG process from start to finish, including the value dossier under § 35a SGB V and the reimbursement price negotiations with GKV-Spitzenverband under § 130b SGB V.

• Lead regional market access initiatives by engaging with sickness funds, the Medical Service, regional physicians’ associations, hospitals, and treatment centers.

• Plan, allocate resources, ensure quality, and submit AMNOG value dossiers to the G-BA.

• Prepare requests for scientific advice, participate in written comment procedures and oral hearings, and manage procedural communications and timelines.

• Develop pricing strategies, negotiation mandates, scenarios, and conduct European reference price analyses.

• Engage with federal and regional payers regarding reimbursement, cost-efficiency reviews, and prior authorization practices.

• Provide guidance to treatment centers on NUB applications, DRG and additional payment mapping, budget and price negotiations, drug committees, and formulary listings.

• Manage individual reimbursement requests, address denials, and handle claw-backs.

• Oversee reimbursement submissions in Austria and Switzerland.

• Integrate market access requirements into study design, evidence planning, and launch strategies.

⛳️ Requirements

• Degree in health economics, pharmacy, medicine, life sciences, or a related field.

• 5–8 years of experience in market access or HTA.

• Proven experience in preparing AMNOG value dossiers under § 35a SGB V, ideally with project lead experience in at least one complete procedure.

• Direct involvement in reimbursement price negotiations under § 130b SGB V.

• Strong understanding of G-BA and IQWiG methodologies, procedural rules, and statutory timelines.

• Ability to critically evaluate clinical evidence and effectively translate it into payer-ready arguments.

• Experience engaging directly with payers and/or hospitals on reimbursement issues.

• Familiarity with German hospital financing mechanisms (NUB, DRG, additional payments).

• Knowledge of reimbursement processes in Austria and Switzerland is a significant advantage.

• Excellent written argumentation skills and the ability to work independently.

• Experience with orphan drugs or a limited evidence base is beneficial.

• Proficient in both German and English.

• Willingness to travel approximately 20% of working time.

🏝️ Benefits

• Competitive compensation package.

• Flexible hybrid work model.

• Opportunities for career growth through regular feedback, continuous education, and professional development programs.

• Financial incentives, peer recognition, and opportunities for advancement.

• Flexible paid time off with a “take-what-you-need” policy and company-paid holidays.

• Comprehensive paid medical and parental leave.

• Access to professional development programs through LinkedIn Learning, LifeLabs, and BetterUp Coaching.

• Opportunities for internal mobility and skill enhancement.

• Approximately 20% travel is expected.