Senior Manager, Epidemiology & Real World Evidence Sciences

Main responsibilities

Epidemiology Support

• Support External Innovation and Business Development teams in the assessment of external licensing opportunities by providing timely disease population assessments.
• Lead and support the development of epidemiologic and real-world evidence assessments to address key business, development, regulatory, safety and market access questions across the product lifecycle.
• Coordinate and contribute to integrated Benefit-Risk (BR) assessments by synthesizing epidemiology, natural history data, clinical trial data, real-world evidence, safety information, unmet need, and patient context to support strategic decision-making.

Project Management/Administrative Support

• Support the coordination and execution of epidemiology data requests and Benefit-Risk (BR) assessments, contributing to evidence generation activities and ensuring timely delivery of high-quality scientific outputs.
• Collaborate with internal stakeholders, external vendors, consultants, and research partners to support epidemiology assessments, evidence syntheses, BR evaluations, and related projects.

Collaborate with Internal Ipsen Stakeholders on All Topics around Epidemiology & RWE

• Collaborate with cross-functional stakeholders (GPS, HEOR, Regulatory, Clinical Development, Medical Affairs, External Innovation, and affiliates) to support EpiCenter requests and Benefit-Risk (BR) assessments.
• Contribute to scientific deliverables, including epidemiology assessments, BR reports, regulatory documents, conference presentations, abstracts, and publications.
• Support the integration of epidemiologic evidence, real-world data, and literature findings into strategic, regulatory, safety, and business decision-making.

Qualifications

• Extensive experience in Epidemiology or Observational Research, including experience within the biotech or pharmaceutical industry.
• Knowledge of medical, regulatory, and payer systems in one or more regions of the world.
• Strong experience in designing and conducting pharmaco-epidemiology studies in support of pre-/post-approval evidence-generating activities.
• Expert in data collection methods and strong familiarity with secondary data sources.
• Experience leading external analytic and evidence-generating activities.
• Proficiency in statistical software and analytical tools (R, SAS, SQL or equivalent)
• Extensive experience working with large healthcare databases and real-world data sources.
• Advanced degree (Master's, MPH, PharmD, PhD, or equivalent) in Epidemiology, Public Health, Biostatistics or a related quantitative health science discipline.
• Additional training or demonstrated expertise in epidemiology, real-world evidence (RWE), observational research, or pharmacoepidemiology is preferred.
• Fluent in English.

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