Health Economics & Payer Evidence Lead- Early Assets Solid Tumours

Role Summary

Health Economics & Payer Evidence Lead- Early Assets Solid Tumours

Responsibilities

• Develop detailed strategic and tactical planning of payer evidence (e.g., clinical trial design and analysis, economic modelling, evidence synthesis including indirect treatment comparisons) to support market access and reimbursement for assigned projects.
• Ensure that the Payer Evidence Strategy & Plan (PESP) is developed and/or validated at each investment decision with key internal and external stakeholders, that it meets the needs of key markets, EU JCA and respective payer archetypes, aligned with the clinical, medical, and brand strategies, and endorsed by all relevant governance bodies.
• Secure cross-functional input to the PESP including real world evidence (RWE) and patient reported outcomes (PROs) for payer needs.
• Plan budgets effectively and secure resources to deliver the evidence required for patient access as outlined in the PESP.
• Deliver assigned projects to time, budget, and quality, including the management of vendors as required.
• Provide payer relevant evidence requirements into the product development plan, including TPP, Phase 3, RWE/observational studies, integrated evidence plan, and post-launch data planning (anticipating key payer requirements) ensuring its implementation/delivery and communication.
• Drive the brand, policy & publication strategies to support payer needs Prepare requests for proposals for outsourced health economics / payer evidence projects and manage the vendor selection process.

Qualifications

• Bachelor’s degree in relevant area, such as health economics or a related quantitative discipline.
• 5 years of market access experience
• Oncology therapy area experience.
• Local or global market access launch experience, having worked at a senior level within a health economic consultancy or several years in a pharmaceutical company (either at a marketing company/local affiliate or global level).
• Effective communication skills to different audiences, including both scientific and commercial.
• Influencing, business acumen, and effective prioritisation skills
• Ability to work both collaboratively and independently, understand and apply different technical approaches, and have a wide understanding of different HTA systems.

Desirable for the role

• Master’s degree or higher education in a relevant area.
• Global market access launch experience and global payer evidence development experience.
• Substantial therapy area experience for the role.
• Can demonstrate an in depth and practical understanding of innovative study methodologies, including analyses, that incorporates clinical, medical, regulatory, commercial, payer and HTA needs.

Additional Requirements

• Office Working Requirements: In-person working a minimum of three days per week from the office.