Jobs at Regeneron

Leads European market access, pricing, reimbursement, and health technology assessment strategies for a neurology pharmaceutical portfolio. Monitors payer and policy trends, supports evidence generation and economic modeling, develops payer value propositions, and participates in negotiations and stakeholder engagement. The role represents Europe in global access planning and collaborates with regional and local teams. It requires extensive pharmaceutical and market access experience, European launch expertise, and knowledge of payer systems.

Leads European rare disease market access strategies, including pricing, reimbursement, health technology assessment submissions, payer engagement, and patient access initiatives. Partners with global, regional, medical affairs, and local teams to develop evidence plans, value propositions, pricing negotiations, and reimbursement strategies across European markets. Requires extensive pharmaceutical market access experience, rare disease expertise, knowledge of payer systems and economic models, and strong stakeholder leadership skills.

Owns global procurement process architecture, standardization, governance, compliance, and continuous improvement across categories and geographies. Partners with procurement technology, Finance, Legal, Compliance, and Quality teams to optimize workflows, automate processes, resolve escalations, and improve user experience. Leads diagnostics, gap assessments, training, change management, communications, and adoption of global procurement practices.

Leads risk-based quality management across global clinical trials, including quality risk assessments, control tracking, issue management, CAPA, trend analysis, inspection readiness, and audit responses. Partners with study teams, monitoring groups, and contract research organizations to manage site risks and escalate significant quality events. Also oversees team onboarding, coaching, performance discussions, and administration.

Leads risk-based Good Clinical Practice audits across internal and external global activities, including scheduling, execution, reporting, and follow-up. Develops audit programs, identifies compliance issues, drives process improvements, supports regulatory inspections, and represents Quality Assurance on complex initiatives. The role requires strong knowledge of FDA, EU, ICH, and GCP requirements, stakeholder leadership, and willingness to travel domestically and internationally.