Global Access Evidence Lead

At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters. The Position We are Roche, committed to advancing science so that we all have more time with the people we love. Our Global Pharma Strategy (GPS) team plays a pivotal role in shaping the future of healthcare by driving the strategic direction of our innovative product portfolio. As a member of the GPS team, you will be at the forefront of transforming groundbreaking scientific discoveries into accessible and impactful healthcare solutions for patients worldwide. We are seeking a dynamic and transformative professional who thrives in a collaborative environment and is passionate about making a difference. The Global Access (GA) department plays a vital role at the intersection of science, access, and innovation. We are dedicated to ensuring that Roche's innovative offerings reach the patients who need them most by shaping how evidence informs patient access across global markets. Our team collaborates across the global organization (commercial and development) and local market access representatives to develop the Access Evidence strategies that support reimbursement and access decisions. We are currently seeking a highly skilled Global Access Evidence Lead with expertise in evidence synthesis and statistical analysis to join our Global Access Evidence Chapter. Reporting to a Global Access Evidence Team Enabler, this role is critical in developing the Access Evidence packages that support key payer and Health Technology Assessment (HTA) body decisions both pre-launch and at the time of product launch. You will play a pivotal role in strengthening Roche’s evidence foundation for today’s HTA challenges and tomorrow’s EU HTA opportunities. The Opportunity - Design and Implement HTA Evidentiary Strategies: Develop evidence to support HTA decision-making, including conducting/leading systematic reviews, feasibility assessments, network meta-analyses, statistical analyses of clinical trial data, and developing indirect treatment comparisons (ITCs). - Provide Strategic Input into Clinical Development: Ensure evidence needs for HTA are considered early in global development and commercialization strategies, providing input into the design of clinical programs. - Develop Access Evidence Packages: Lead the synthesis and preparation of evidence, including literature reviews, to support HTA submissions, and lead the development of global access evidence and/or Joint Clinical Assessment (JCA) dossiers with cross-functional teams and vendor support. - Contribute to EU HTA Readiness: Develop evidence strategies and synthesis approaches that anticipate JCA requirements in preparation for the EU HTA Regulation. - Manage External Partners: Be accountable for managing external agencies to ensure the timely delivery of high-quality, consistent, and compliant access deliverables. - Maintain Strategic Alignment & Expertise: Ensure functional activities align with the wider organization and stay current with the changing HTA landscape, academic research areas, and novel methodologies. - Communicate Evidence Insights: Communicate clear integrated access evidence strategies, methodologies, and insights derived from evidence used within HTA to diverse audiences, linking evidence impact to broader access and commercialization strategies. Who You Are - Education: Hold a Masters or Doctoral level degree (MD, PharmD, PhD in health economics, epidemiology, statistics, mathematics, public health, or life science disciplines are preferred). - HTA & Evidence Expertise: Demonstrate extensive knowledge of health technology assessment, clinical research and development methods, and international payer evidence requirements, with a proven ability to critically evaluate and synthesize data from multiple sources using established methodologies for systematic literature reviews (SLRs). - Experience: Preferably, you possess 3 or more years’ experience in the pharmaceutical or related industry, working successfully within a highly matrixed environment, with previous experience in product development, regulatory, medical affairs, or an access function. - Skills & Mindset: Exhibit strong strategic, collaboration, and communication skills (written and verbal English), along with a solution-driven and open mindset to adopt digital technologies for work. A track record of high-quality research publications is beneficial. - Collaboration: A committed team player who can work effectively with all key stakeholders, including both local and global colleagues. - Track record of research publications and other research outputs of high quality is beneficial Who we are A healthier future drives us to innovate. Together, more than 100’000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact. Let’s build a healthier future, together. Roche is an Equal Opportunity Employer.