PDMA Evidence Solution Leader

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The Position

The Evidence Solution Leader (ESL) is a critical role within Product Development Medical Affairs (PDMA), responsible for designing and enabling strategic evidence solutions to address prioritized gaps identified in the Integrated Evidence Plan (IEP).

This is a strategic medical role that provides expertise in insight generation, evidence generation, scientific engagement, and affiliate enablement, with a focus on optimizing evidence solution design. By maximizing data utility, enhancing the value proposition of therapies, and increasing the visibility and impact of real-world evidence, the ESL ensures evidence strategies are grounded in foresight and tailored to the evolving needs of patients, healthcare professionals, and decision-makers.

• You serve as a medical and methodological expert for RWD and data reuse, supporting prioritized DAs, asset teams, and affiliates
• You lead the design of evidence solutions that are fit-for-purpose, decision-driven, and aligned with strategic priorities across the lifecycle
• You contribute to IEPs by recommending optimal solutions, including reuse of data assets, NIS and RWD scientific projects
• You proactively identify and drive opportunities for data reuse across studies, systems, and geographies and promote transparency of internal data assets and tools that enable future reuse
• You partner with cross-functional stakeholders (medical, access, clinical, commercial, data science) and affiliates to align on evidence needs and feasibility.
• You enable affiliates by co-creating local and multi-country evidence solutions, sharing expertise, and promoting use of standardized frameworks and tools (e.g., EVAL, evidence atlas)
• You create and sustain a community of local Evidence Generation Leaders focused on capability building, data landscaping, RWD initiatives, and data reuse

• You have an advanced degree in a relevant scientific field (MD, PhD, PharmD, or equivalent in life sciences, epidemiology, public health, health economics, or related discipline) with 7+ years of experience in the pharmaceutical, biotechnology, or healthcare industry, with at least 3–5 years in evidence generation, real-world data (RWD), or non-interventional study (NIS) leadership roles
• You have demonstrated experience contributing to or leading integrated evidence plans (IEPs) or equivalent cross-functional strategic planning
• You have global or multi-country experience in medical affairs, clinical development, health outcomes, or RWE preferred
• You have a deep understanding of real-world evidence methodologies, including study design, data sources (EHR, claims, registries, etc.), analysis approaches, and interpretation
• You have knowledge of data privacy, governance, and regulatory frameworks governing RWD generation and use across major markets (e.g., US, EU, APAC)
• You have working knowledge of health authority and HTA evidence expectations (e.g., EMA, FDA, NICE, G-BA, CADTH), particularly where RWE contributes to demonstrating treatment value, real-world effectiveness, or addressing uncertainties in clinical trials
• You have proficiency with medical evidence planning and insight-generation tools, including structured evidence planning frameworks, RWD portals, and data catalogs used to identify and evaluate internal and external evidence assets
• You have experience in developing and managing NIS, RWD, and data reuse projects, including protocol development and result dissemination

Posting: until Oct 1

Are you ready to apply? We want someone who thinks beyond the job offered - someone who knows that this position can be a unique opportunity to shape the future of Roche.

Who we are

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.