The Opportunity Lead EU HTA evidence strategy : Shape Roche's approach to EU HTA submissions by embedding sophisticated, anticipatory evidence strategies into clinical development from inception, ensuring alignment with EMA regulations, and the new EU HTA regulations. Position us as a benchmark for evidence excellence across European markets. Drive methodological innovation in EU contexts : Leverage your established networks within European HTA bodies, payers, and health authorities to advance evidence standards and best practices—influencing how the industry approaches submissions to national HTA organizations and contributing to the evolution of EU HTA frameworks. Architect compelling EU submissions : Design innovative, region-specific evidence packages that anticipate the needs of EMA committees, HTA bodies and national payers. Identify strategic evidence gaps early, pioneer novel data sources and analyses, and translate complex statistical findings into narratives that drive reimbursement and access decisions across EU markets. Establish Roche as an EU HTA expert : Leverage your reputation and deep relationships within the European Access/HTA ecosystem to elevate submission quality, engage proactively with key opinion leaders and HTA bodies, and position Roche as a thought leader in EU evidence generation and submission strategy. Lead strategic statistical analysis for EU evidence packages : Lead and critically evaluate complex statistical analyses—including network meta-analyses and real-world evidence syntheses—ensuring methodological rigor and compliance with EU HTA requirements while translating findings into compelling, region-appropriate narratives. Enable affiliates and cross-functional teams : Guide European affiliate teams and cross-functional partners in building robust EU submission strategies, ensure alignment across EMA development pathways and national HTA submissions, and mentor colleagues on evolving EU regulatory and HTA landscapes. Contribute to EU HTA evolution : Maintain influential engagement with European HTA bodies, regulatory agencies, and academic networks—actively participating in professional forums, contributing to methodological debates, and ensuring Roche remains at the forefront of EU evidence standards and innovation.
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