Associate Director, HEOR & Market Access, EU West

Mavericks Wanted When was the last time you achieved the impossible? If that thought feels overwhelming, you might want to pause here, but if it sparks excitement...read on   In 2015, we pioneered a “moneyball for biotech” approach, pooling projects and promising early-stage research from academia together under one financial umbrella to reduce risk and unleash innovation. This model allows science and small teams of experts to lead the way. We build bridges to groundbreaking advancements in rare disease, and develop life-changing medicines for patients with unmet needs as fast as humanly possible.    Together we define white space, push boundaries, and empower people to solve problems. If you're someone who defies convention, join us and work alongside some of the most respected minds in the industry. Together, we'll ask "why not?" and help reengineer the future of biopharma. At BridgeBio, we value curiosity and experimentation—including the ethical & thoughtful use of AI to improve clarity, speed, and quality of work. What You’ll Do You will report to the Senior Director, Head of Market Access, EU West Region and work closely with Medical affairs, Market Access, Commercial locally and globally, to support BridgeBio’s mission of delivering transformative medicines to patients with genetic rare diseases. You will own the value demonstration strategy for our products across the region, and translate it into effective patient access: design each product's evidence generation plan, drive it through to delivery, and align it with pricing and access strategy, starting in France, then extending to the other countries of the EU West region Your main responsibilities include: Evidence generation Design and lead natural history studies, cohorts, registries, and analyses of medico-administrative databases (SNDS, BNDMR/ BaMaRa, rare disease network registries) Lead indirect comparisons in the context of single-arm trials and very small patient populations Develop health economic models (cost-effectiveness, budget impact) for France, then for other markets in the region Design real-world data collection frameworks (PUT-RD / data collection protocols) that can be reused for reassessment and in other countries Define the scientific publication and communication plan Study management Draft specifications, run tenders, and select vendors Convene and lead external scientific advisory committees Secure all required approvals (health data access, ethics committees, regulatory compliance) Manage the administrative, contractual, and budgetary aspects of studies Review and validate all deliverables (protocols, analysis plans, study reports, publications) Value communication and internal expertise Translate study results into actionable clinical and economic arguments Drive scientific dissemination (congresses, publications) Serve as the internal reference point on epidemiology, health economics, and health data matters Build and maintain a network of research agencies, academics, and institutions Value and access strategy Define and own the value demonstration strategy for each product across the region Build economic value propositions and value dossiers and ensure their local adaptation Contribute to pricing strategy and preparation for CEPS negotiations (e.g., positive externalities, budget impact) Coordinate and build the economic modelling and CEESP dossier (early scientific advice, modelling, CEESP submission, technical exchange, etc.) Contribute the health-economic and RWE content of early access dossiers and submissions to the Transparency Committee, in coordination with the Market Access Director, with progressively increasing ownership of Benelux dossiers Anticipate assessors' objections and build responses ahead of submission French rare disease ecosystem Build working relationships with rare disease networks, reference and competence centres,