Europe Joint Health Technology Assessment Lead

Vor 6 Tagen

Zurich, Schweiz Takeda Pharmaceutical Vollzeit

Our team is growing and for this we need bright minds with creativity and flexibility - **what talent do you have?**

For our Oncology Patient Value, Policy and Access team at our European HQ in Zürich, Switzerland we are looking for a **Europe Joint Health Technology Assessment Lead** and you will be in the forefront of the new regulation that will be the future.

For this role you can be based in any country in Europe, and you can expect 25% domestic and or international travel in Europe.

You will be responsible for overseeing the execution of the European Union Joint Health Technology Assessment (HTA) submissions and leading the Takeda Oncology relationship with the EU HTA agency, the HTA Coordination Group (HTACG). Additionally, you will be providing continuous input as an expert on EU Joint HTA guidelines, methods, and processes to shape the market access strategy and clinical development plan across Takeda’s oncology portfolio.

To succeed in this role, we are looking for your ability to collaborate and partner with the PVPA team and internal cross-functional stakeholders to design the future ways of working with local, regional, and global teams which embed the new EU HTA procedures within our operating model.

**ACCOUNTABILITIES**
- Co-lead the strategy and development of high quality HTA government submission dossiers for the European Union Join Clinical Assessments (JCA) and Joint Scientific Consultations (JSC) for new oncology medicines with the EUCAN Access Lead.
- Lead internal expert on the methodological requirements and specifications for the EU HTA procedures and methods.
- Shape relationships with EU government agencies responsible for HTA and act as the primary point of contact, representing Takeda in communications and negotiations with EU HTA Coordination Group and related key stakeholders.
- Responsibility for coordinating the external stakeholder engagement process for JCA submissions in collaboration with EUCAN access lead, EUCAN medical, patient advocacy and country affiliates.
- In collaboration with the EUCAN Access Lead:

- Co-leads the EU JCA submission teams, leveraging expertise and collaborating closely with regional, global and LOC members of access/HEOR and key cross-functional teams,
- Co-leads Joint Scientific Consultation to collect feedback on clinical trial considerations to inform clinical development and evidence generation strategies.
- As a key member of the Payer Value and Patient Access (PVPA) sub-team, responsible for representing the joint EU HTA archetype in internal regional and global forums including communicating requirements and changes in EU joint HTA guidelines to inform the global brand, PVPA functional plan and the asset clinical development plans.
- Develop and manage strong relationships with EU key opinion leaders, HTA/payers, academic researchers, and vendors to ensure excellence in JCA and JSC activities, validation of the market access strategy and dossier assumptions.
- Responsible for leading internal communication and educating internal stakeholders on key developments on EU Joint HTA including procedure and method guideline updates.
- Responsible for understanding trends, relationships/influence and collaboration of national HTA/payers, regulatory agencies (EMA) with the EU HTA CG and provide these strategic insights to global PVPA. Based on these insights, shape EU joint HTA and reimbursement strategies.

**EDUCATION, BEHAVIOURAL COMPETENCIES AND SKILLS**
- Minimum bachelor’s degree, advanced / graduate degree (MSc, PhD, MPH, MPP, MBA) preferred.
- Minimum of 8 years’ experience in healthcare consulting or biopharmaceuticals industry
- Minimum of 5 years’ experience in market access, health economics, pricing, health policy, public health, and/or international affairs showcasing increasing responsibility and experience in the same or similar roles; local affiliate experience is a plus.
- Previous direct experience leading a national Health Technology Assessment (HTA) submission including leading the submission team, developing a dossier, setting the submission strategy and stakeholder engagement plan; EUnetHTA experience is a plus.
- Ability to think strategically with strong leadership, influencing, collaboration, and communication skills.
- Strong understanding of the EU payer environment, HTA trends and reimbursement guidance and technical methodologies (NCPE, TLV, G-BA, HAS, NICE, EUnetHTA, etc.) - such as health economics, reimbursement authorities’ decision-making processes, and current issues.
- Previous experience in Oncology is a plus.
- Expertise in health technology assessment tools, value materials, methods, evidence synthesis approaches (indirect treatment comparisons, network meta-analyses) and clinical and HTA/payer insight elicitation (i.e. advisory board).
- Demonstrated strong verbal and written communication skills - previous experience with external stakeholder management, communication with HTA or reimbursem

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