Senior Director, HEOR, Europe
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Job Location:
Basel - Switzerland
Monthly Salary:
Not Disclosed
Posted on:
Yesterday
Vacancies:
1 Vacancy
Job Summary
Revolution Medicines is a clinical-stage precision oncology company focused on developing novel targeted therapies to inhibit frontier targets in RAS-addicted cancers. The companys R&D pipeline comprises RAS(ON) Inhibitors designed to suppress diverse oncogenic variants of RAS proteins and RAS Companion Inhibitors for use in combination treatment strategies. As a new member of the Revolution Medicines team you will join other outstanding Revolutionaries in a tireless commitment to patients with cancers harboring mutations in the RAS signaling pathway.
The Opportunity:
The Senior Director HEOR Europe will participate in developing the strategy and then driving execution of the tactical plan across health economics outcomes research and real-world evidence (RWE) to optimize the value demonstration of the Revolution Medicines oncology portfolio across European markets. They will work in concert with the Global HEOR and other regional teams to deliver an impactful evidence for select assets and disease areas. The Senior Director HEOR Europe will work across the European Matrix including Medical Affairs Market Access Commercial and Country level teams. The Senior Director HEOR Europe will report to the Executive Director HEOR Europe and will be part of the broader extended Global HEOR/RWE and IEP team. They will participate with cross-Europe initiatives and be responsible for leading target projects and may be accountable for Global alignment on select programs.
Key Responsibilities
Strategic Leadership:Working with the Executive Director HEOR Europe and the Global HEOR team will provide insights and represent the EU on initiatives from Discovery to late life cycle.
Implement HEOR strategy across Europe in support of product lifecycle planning value evidence generation pricing/reimbursement and access engagements. Support JCA preparation and dossier development as well as HTA engagement and preparation
Integrated Evidence Planning: Participate from Europe within the Revolution Medicines IEP process and ensure the comprehensive plan achieves all needs for the EU markets.
Evidence Generation & Analysis:Lead development of asset specific health economic models (cost-effectiveness budget impact) real-world evidence burden-of-disease assessments and outcomes research programs that support regulatory filings HTA submissions and payer discussions.
Cross-Functional Collaboration:Partner with Market Access Medical Affairs Commercial Regulatory and Clinical Development teams to ensure HEOR insights inform decision making across the product lifecycle.
External Engagement:Represent Revolution Medicines in scientific payer and HTA forums; engage external stakeholders including key opinion leaders academic collaborators HTA bodies and payers.
Team & Vendor Leadership:Provide asset specific project leadership to teams tasked with evidence generation across key markets; manage external collaborators (consultants vendors) to support various HEOR projects within budget and timelines.
Communication:Support the communication of HEOR strategy research outcomes and value propositions to internal leadership (including European and global functions) and external audiences.
Required Skills Experience and Education:
Advanced degree (PhD MSc MPH or equivalent) in Health Economics Epidemiology Pharmacoeconomics Biostatistics Public Health or related discipline.
12 years experience working in the pharmaceutical industry.
Extensive HEOR experience (>7-10 years) in pharmaceutical/biotech/consulting settings with significant leadership exposure.
Demonstrated expertise in health economic modeling RWE study design outcomes research methodologies and HTA submission experience.
Strong scientific credibility strategic vision and ability to influence cross-functional and external stakeholders
Excellent communication and leadership skills with experience presenting at scientific and payer forums.
Preferred Skills:
Demonstrated ability to drive success through cross-functional team leadership and team motivation.
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Required Experience:
Exec
Key Skills
- FDA Regulations
- Management Experience
- Manufacturing & Controls
- Biotechnology
- Clinical Development
- Clinical Trials
- Drug Discovery
- Project Management
- Filing
- Team Management
- Leadership Experience
- Chemistry
