About Philip
English
Native or bilingual
Experience
- INDEPENDENT LIFEAdvisorPHARMACEUTICALS INDUSTRYJanuary 2026 - Today (5 months)London, UK• • Fractional Executive Leadership & Interim Management: Providing immediate, "plug-and-play" senior leadership (e.g., Interim VP of Market Access / Fractional Chief Commercial Officer) to biopharma companies to ensure strategic continuity during critical hiring gaps and continual market access strategy development.• • Commercial Due Diligence (CDD) & Asset Valuation: Partnering with Private Equity, Venture Capital, and biopharma BD&L teams to deliver rapid, rigorous asset valuations—assessing market access viability, pricing potential, and peak revenue to de-risk high-stakes M&A and licensing transactions.• • Global Pricing Governance & Launch Readiness: Architecting end-to-end market access strategies andcompelling payer value propositions to seamlessly transition specialized assets (Orphan/Rare, Immunology, Oncology) from Phase II/III clinical trials to successful commercial launch.
- EY-PARTHENON,Partner – Commercial & Market Access Service Lines LeadPHARMACEUTICALS INDUSTRYJanuary 2023 - January 2026 (3 years)London, UK• • Market Access Practice Leadership: Directed a team of 20+ specialists, acting as the senior strategic advisor to mid- and large-cap biopharma C-suites on complex global launch, pricing, and mandates.• • Asset Commercialization & Risk Mitigation: Spearheaded comprehensive global pricing strategies, P&R risk assessments, and go-to-market plans, directly maximizing peak revenue potential for highly specialized clinical assets.• • Responsible for comprehensive global pricing strategy, risk assessments, supporting client go-to-market plans, and driving revenue maximization globally.• • Key
- CSL VIFOR,Global Head of Pricing & Market Access – OrphanPHARMACEUTICALS INDUSTRYJanuary 2021 - January 2023 (2 years)Zürich, Switzerland• • Oversaw market access strategy and implementation for the largest portfolio in the company ($500M) – the orphan disease franchise – while holding a dual role as Senior Director of Business Development & Licensing.• • Worked across stakeholders (medical, marketing, regulatory, clinical) to create compelling value propositions and competitive access strategies for rare disease products.• • Implemented new internal corporate processes and pricing governance to better align the company to industry standards; established a toolkit with a standardized set of deliverables to achieve low variability across markets.• • Explored alternative pathways for early payer engagement, such as the Mechanism for Orphan Coordinated Access (MoCA), creating education opportunities to preempt key questions and streamline formal HTA assessments.
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Education
- Doctor of PhilosophyUniversity College London2006Doctor of Philosophy
- Bachelor of ScienceUniversity of Manchester2002Bachelor of Science