Takeda
Qdenga Market Access & Payer Value Head(m/w/x)
Full-timeOn-siteSenior
Zürich
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TATakeda Pharmaceuticals International AG
Europe Health Technology Assessment Associate Lead(m/w/x)
Zürich
Full-timeOn-siteSenior
Nejo AI Summary
Co-leading EU HTA document preparation for oncology pharmaceuticals at a specialty pharmaceutical developer, synthesizing evidence from PICO surveys. 6+ years in biopharma/healthcare consulting and 4+ years in market access/HEOR, with strong EU HTA understanding, required. Extensive international collaboration across European HTA stakeholders.
Requirements
- Bachelor’s degree, advanced/graduate degree preferred
- Minimum of 6 years’ experience in biopharmaceuticals industry or healthcare consulting
- Minimum of 4 years’ experience in market access, health economics, pricing, health policy, outcomes research, or consulting
- Strong understanding of EU payer and HTA environment
- Advanced verbal and written communication, presentation and influencing skills
- Ability to manage complex projects with multiple stakeholders
- Solid knowledge of drug development processes
- Ability to navigate ambiguity and complex trade-offs
- Ability to frame HTA strategies and arguments
- Hands-on experience in health technology assessment tools
- Advanced/graduate degree (MSc, PhD, MPH, MPP, MBA)
- Degree or diploma in health economics or economic evaluations
- Previous experience in Oncology
- Previous experience in an above country role
- Direct experience leading national HTA submissions or early scientific advice
- 20% Domestic and/or International travel required
- Prior experience in assessing evidence needs for major HTA/payer stakeholders
- Excellent collaboration and communication skills
- Experience in internal stakeholder management and a solution mindset
- Strong understanding of clinical development process
Tasks
- Collaborate with regional access leads to identify evidence needs from HTA stakeholders across Europe
- Gather and synthesize evidence for EU HTA-related projects, including PICO surveys and data consolidation
- Support the development of market access strategies and clinical development plans for Takeda’s oncology portfolio
- Co-lead the preparation and submission of EU Health Technology Assessment documents, ensuring compliance with EU guidelines
- Promote Takeda’s values and foster collaboration with cross-functional and global partners
- Co-lead the strategy and development of high-quality HTA submission dossiers for new oncology medicines
- Ensure timely completion of comprehensive HTA and payer evidence requirement mapping via PICO simulations
- Represent joint EU HTA archetype’s evidence needs in internal regional and global forums
- Co-lead Joint Scientific Consultations to gather feedback on clinical trial considerations
- Serve as the single point of contact for all JCA and JSC related evidence topics for assigned assets
- Guide internal stakeholders on methodological requirements for EU HTA Regulation methods and procedures
- Maintain up-to-date knowledge of EU HTA guidelines, methods, and processes
- Provide strategic insights on trends and collaborations of national HTA/payers and regulatory agencies
Work Experience
- 6 years
Education
- Vocational certificationOR
- Bachelor's degreeOR
- Master's degree
Languages
- English – Business Fluent
Find the original job posting in its most current version here. Nejo automatically captured this job from the website of Takeda Pharmaceuticals International AG and processed the information on Nejo with the help of AI for you. Despite careful analysis, some information may be incomplete or inaccurate. Please always verify all details in the original posting! Content and copyrights of the original posting belong to the advertising company.
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TATakeda Pharmaceuticals International AG
Europe Health Technology Assessment Associate Lead(m/w/x)
Zürich
Full-timeOn-siteSenior
Nejo AI Summary
Co-leading EU HTA document preparation for oncology pharmaceuticals at a specialty pharmaceutical developer, synthesizing evidence from PICO surveys. 6+ years in biopharma/healthcare consulting and 4+ years in market access/HEOR, with strong EU HTA understanding, required. Extensive international collaboration across European HTA stakeholders.
Requirements
- Bachelor’s degree, advanced/graduate degree preferred
- Minimum of 6 years’ experience in biopharmaceuticals industry or healthcare consulting
- Minimum of 4 years’ experience in market access, health economics, pricing, health policy, outcomes research, or consulting
- Strong understanding of EU payer and HTA environment
- Advanced verbal and written communication, presentation and influencing skills
- Ability to manage complex projects with multiple stakeholders
- Solid knowledge of drug development processes
- Ability to navigate ambiguity and complex trade-offs
- Ability to frame HTA strategies and arguments
- Hands-on experience in health technology assessment tools
- Advanced/graduate degree (MSc, PhD, MPH, MPP, MBA)
- Degree or diploma in health economics or economic evaluations
- Previous experience in Oncology
- Previous experience in an above country role
- Direct experience leading national HTA submissions or early scientific advice
- 20% Domestic and/or International travel required
- Prior experience in assessing evidence needs for major HTA/payer stakeholders
- Excellent collaboration and communication skills
- Experience in internal stakeholder management and a solution mindset
- Strong understanding of clinical development process
Tasks
- Collaborate with regional access leads to identify evidence needs from HTA stakeholders across Europe
- Gather and synthesize evidence for EU HTA-related projects, including PICO surveys and data consolidation
- Support the development of market access strategies and clinical development plans for Takeda’s oncology portfolio
- Co-lead the preparation and submission of EU Health Technology Assessment documents, ensuring compliance with EU guidelines
- Promote Takeda’s values and foster collaboration with cross-functional and global partners
- Co-lead the strategy and development of high-quality HTA submission dossiers for new oncology medicines
- Ensure timely completion of comprehensive HTA and payer evidence requirement mapping via PICO simulations
- Represent joint EU HTA archetype’s evidence needs in internal regional and global forums
- Co-lead Joint Scientific Consultations to gather feedback on clinical trial considerations
- Serve as the single point of contact for all JCA and JSC related evidence topics for assigned assets
- Guide internal stakeholders on methodological requirements for EU HTA Regulation methods and procedures
- Maintain up-to-date knowledge of EU HTA guidelines, methods, and processes
- Provide strategic insights on trends and collaborations of national HTA/payers and regulatory agencies
Work Experience
- 6 years
Education
- Vocational certificationOR
- Bachelor's degreeOR
- Master's degree
Languages
- English – Business Fluent
Find the original job posting in its most current version here. Nejo automatically captured this job from the website of Takeda Pharmaceuticals International AG and processed the information on Nejo with the help of AI for you. Despite careful analysis, some information may be incomplete or inaccurate. Please always verify all details in the original posting! Content and copyrights of the original posting belong to the advertising company.
About the Company
Takeda Pharmaceuticals International AG
Industry
Pharmaceuticals
Description
The company is transforming patient care through the development of novel specialty pharmaceuticals and best in class patient support programs.
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