.(LFF977) | Advisor/Director Real World Evidence (RWE) - OncologyWe're looking for people who are determined to make life better for people around the world.The demand for high quality health economic and outcomes research (HEOR) and real-world evidence (RWE) to support drug development, health technology assessment/access decisions, product differentiation, and clinical decision making continues to increase.The purpose of the Lilly Value, Evidence, and Outcomes (VEO) team is to accelerate equitable patient access and transform healthcare delivery through the execution and communication of bold, high impact science.We are looking for talented, energetic, creative, diverse, influential, and collaborative team members to join the VEO function and Team Lilly.The VEO-International RWE scientist will provide strategic insight/leadership into the Real World Evidence (RWE) for Lilly's oncology portfolio.The scientist will use their knowledge of health outcomes disciplines, therapeutic area knowledge of oncology, understanding of drug development and commercialization, and geographic market knowledge in the role.Research project ownership and execution is required. The scientist may have duties ranging from developing and articulating product value propositions, patient reported outcomes strategies, real world evidence generation, and differentiation strategies using RWE research.Primary Responsibilities:Strategy: Drives sustained integration of RWE from early clinical development through commercialization.Develops and oversees RWE research strategy for compounds in the Lilly portfolio in the relevant therapeutic area(s).Serves as a strategic partner on lead/core teams throughout development and/or commercialization.Formulates and drives Real World Evidence for priority products and geographies.Study Development and Execution:Develops bold high impact science for products across the lifecycle to influence and support evidence needs for Lilly products in support of improving patient outcomes.Applies technical expertise appropriate for the role (e.G., scope or depth in statistical analysis, clinical trials, observational/epidemiologic research, or other value assessment) within a therapeutic area.Applies disease state knowledge and research methods to generate RWE evidence for registration, pricing, reimbursement, access and other external stakeholders such as healthcare practitioners.Organizational Leadership and Influence:Links technical expertise with business acumen and establishes and maintains strategic relationships with key internal and external decision makers.Effectively leads RWE evidence planning and implementation in collaboration with cross-functional teams across the development and commercialization lifecycle teams.Effectively integrates with and influences key business partners and external stakeholders to achieve goals and outcomes
