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Patient Access Manager DACH (m/w/d) Pre-Launch (DE)

[5872]

Our client is an international speciality healthcare company dedicated to rare diseases with the German presence in Munich. Furthermore the company is a pioneer in biotechnology with world-class capabilities in protein biochemistry and biologics manufacturing. Patient Access Manager DACH (m/w/d) Pre-Launch Ihre Aufgaben ·Working in a cross-functional team to support and develop market access projects in terms of the companies pipeline and launch products ·Operationalize and support/lead the development of Market Access strategies especially in o the preparation of German AMNOG dossiers including analysis and discussion of clinical trial results and their methodology o Analyze product environment and available product data (e.g., AMNOG-Monitoring) ·Support/lead timely submission of relevant pricing and reimbursement dossiers as required in light of current health environment and applicable regulations including but not limited to: oDevelopment of the dossier strategy in close collaboration with the Senior Patient Access Manager oCoordinate cross-functional workstream team and ensure preparation of appropriate AMNOG dossiers  oSupport/lead preparation of (early) G-BA consultations as required oSupport/lead timely submission and best possible preparation and positioning for written statement and oral hearing processes with G-BA during early benefit assessment process oInforming the companies pipeline through targeted evaluation of clinical development programs regarding German access requirements oInforming development of pricing strategy for pipeline and early launch products by analyzing pricing landscape, AMNOG environment and conducting horizon scanning oPreparing for P&R negotiations with local payers, including AMNOG negotiations with GKV-SV ·Propose, coordinate and lead appropriate HEOR or RWE projects to inform pricing strategy, support dossier strategy or value proposition of the products in collaboration with Global patient access or other departments ·Update regularly local and global cross functional teams on environment changes and potential consequences, proposed strategies and ongoing activities related to market access responsibilities in the region Ihre Qualifikationen ·University Degree with at least 3 years of professional experience in a pharmaceutical or biotech or med-tech environment ·Experience in focussing on pricing models and business cases for future products from the pipeline ·Experience in preparing and conducting proce negotiations ·Knowledge of the regional and national market access environment ·Demonstrated ability to propose and execute on a regional strategic plan ·Good communication skills (oral and writing) in German and English ·Solid understanding of commercial, medical functions and back up roles such us (regulatory, legal, financial) and how these roles best contribute to a successful patient access approach If you have any further questions, please contact Mr. Tilman Grumbd at +49 441 21879-34 or via e-mail at tilman.grumbd@optares.de.

Our client is an international speciality healthcare company dedicated to rare diseases with the German presence in Munich. Furthermore the company is a pioneer in biotechnology with world-class capabilities in protein biochemistry and biologics manufacturing.

Patient Access Manager DACH (m/w/d)
Pre-Launch

Ihre Aufgaben
  • Working in a cross-functional team to support and develop market access projects in terms of the companies pipeline and launch products
  • Operationalize and support/lead the development of Market Access strategies especially in o the preparation of German AMNOG dossiers including analysis and discussion of clinical trial results and their methodology o Analyze product environment and available product data (e.g., AMNOG-Monitoring)
  • Support/lead timely submission of relevant pricing and reimbursement dossiers as required in light of current health environment and applicable regulations including but not limited to:
    • Development of the dossier strategy in close collaboration with the Senior Patient Access Manager
    • Coordinate cross-functional workstream team and ensure preparation of appropriate AMNOG dossiers 
    • Support/lead preparation of (early) G-BA consultations as required
    • Support/lead timely submission and best possible preparation and positioning for written statement and oral hearing processes with G-BA during early benefit assessment process
    • Informing the companies pipeline through targeted evaluation of clinical development programs regarding German access requirements
    • Informing development of pricing strategy for pipeline and early launch products by analyzing pricing landscape, AMNOG environment and conducting horizon scanning
    • Preparing for P&R negotiations with local payers, including AMNOG negotiations with GKV-SV
  • Propose, coordinate and lead appropriate HEOR or RWE projects to inform pricing strategy, support dossier strategy or value proposition of the products in collaboration with Global patient access or other departments
  • Update regularly local and global cross functional teams on environment changes and potential consequences, proposed strategies and ongoing activities related to market access responsibilities in the region

Ihre Qualifikationen

  • University Degree with at least 3 years of professional experience in a pharmaceutical or biotech or med-tech environment
  • Experience in focussing on pricing models and business cases for future products from the pipeline
  • Experience in preparing and conducting proce negotiations
  • Knowledge of the regional and national market access environment
  • Demonstrated ability to propose and execute on a regional strategic plan
  • Good communication skills (oral and writing) in German and English
  • Solid understanding of commercial, medical functions and back up roles such us (regulatory, legal, financial) and how these roles best contribute to a successful patient access approach
If you have any further questions, please contact Mr. Tilman Grumbd at +49 441 21879-34 or via e-mail at tilman.grumbd@optares.de. 

map München, Deutschland date_range 11.01.2023 update Permanent
Zulassung
Direct contact

Tilman Grumbd

Geschäftsführer
mail tilman.grumbd@optares.de
phone +49 441 21879-34


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