Basic Qualification We are seeking professionals with the following required skills and qualifications to help us achieve our goals: PhD, DrPH, MD, or other doctoral degree in epidemiology, public health, biostatistics, or a closely related quantitative discipline At least 8 years of experience conducting pharmacoepidemiology or real-world evidence (RWE) studies Experience designing and conducting observational studies (e.g., post-approval studies, real-world evidence generation) Experience leading epidemiology programs supporting clinical development and/or regulatory decision-making Experience within the pharmaceutical, biotechnology, vaccine, or related research environment Experience building and managing or leading teams of scientific or technical professionals Experience authoring or contributing to scientific publications or regulatory documents Preferred Qualification If you have the following characteristics, it would be a plus: Experience in viral and bacterial respiratory diseases Experience interacting with regulatory authorities or supporting regulatory submissions Expertise in advanced epidemiologic methods (e.g., causal inference, machine learning applied to observational data) Demonstrated ability to influence internal and external stakeholders, including scientific and regulatory bodies Strong written and verbal communication skills, including presentation at scientific conferences Experience building strategic external collaborations (e.g., academia, CROs, or consortia) Experience driving innovation, capability building, or organizational change within an epidemiology or RWE function Role Location This role is offered as a hybrid position in the United States, Belgium, United Kingdom or The Netherlands How to apply We want to hear from you. Key Responsibilities Provide strategic leadership in epidemiology and real-world evidence across multiple programs and assets Lead and develop a team of epidemiologists, ensuring high-quality scientific output and delivery Oversee the design and execution of epidemiologic studies, including observational and post-approval studies Partner with cross-functional teams (e.g., clinical sciences, safety, regulatory) to support research and development programs and evidence generation Contribute to governance and strategic decisions at an above-asset level Oversee scientific dissemination, including publications, conference presentations, and regulatory documents Build and maintain external collaborations with academic institutions, consortia, and research organizations Why You?