Job Description

Bei Roche kannst du ganz du selbst sein und wirst fur deine einzigartigen Qualitaten geschatzt. Unsere Kultur fordert personlichen Ausdruck, offenen Dialog und echte Verbindungen. Hier wirst du fur das, was du bist, wertgeschatzt, akzeptiert und respektiert. Dies schafft ein Umfeld, in dem du sowohl personlich als auch beruflich wachsen kannst. Gemeinsam wollen wir Krankheiten vorbeugen, stoppen und heilen und sicherstellen, dass jeder Zugang zur Gesundheitsversorgung hat - heute und in Zukunft. Werde Teil von Roche, wo jede Stimme zahlt.


Die 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 OpportunityDesign 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 AreEducation: 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

Wer wir sind
Eine gesundere Zukunft treibt uns zur Innovation an. Mehr als 100.000 Mitarbeiter weltweit arbeiten gemeinsam daran, wissenschaftliche Fortschritte zu erzielen und sicherzustellen, dass jeder Zugang zur Gesundheitsversorgung hat - heute und fur zukunftige Generationen. Durch unser Engagement werden uber 26 Millionen Menschen mit unseren Medikamenten behandelt und mehr als 30 Milliarden Tests mit unseren Diagnostik-Produkten durchgefuhrt. Wir ermutigen uns gegenseitig, neue Moglichkeiten zu erkunden, Kreativitat zu fordern und hohe Ziele zu setzen, um lebensverandernde Gesundheitslosungen zu liefern.


Gemeinsam konnen wir eine gesundere Zukunft gestalten.

Roche ist ein Arbeitgeber, der die Chancengleichheit fordert.