Senior Manager, Epidemiology & Real World Evidence Sciences Groupe Talents Handicap

At Ipsen, we choose to focus on what matters most. Patients. Progress. Partnership. Yes.

We are looking for a Head of Safety Partnering to define and lead our global pharmacovigilance partnering strategy across a diverse commercial portfolio. This is a pivotal leadership role at the heart of how we collaborate, ensuring that strong partnerships translate into safe, compliant and impactful outcomes for patients worldwide.

Why this role matters

The Senior Manager, Epidemiology and RWE Sciences will work closely with the Director, Pharmacoepidemiology & Patient Centered Outcomes to support pharmacoepidemiologic and various evidence generation activities across the entire product portfolio (Oncology, Rare Diseases and Neuroscience).

You will:

• Oversee generation and explanation of epidemiologic data across the business, supporting the design of evidence generating activities using primary and secondary data, management of epidemiologic benefit-risk evaluations in partnership with the safety team, and support for analytics related to various evidence generation activities across the Epi and RWE team, as neede
• Partner with internal stakeholders across the Asset Team to ensure the availability of robust epidemiologic data and produce data that is medically relevant, scientifically sound and meets Ipsen's commitment of providing Innovation for Patient Care.
• Be responsible for methodological epidemiological & RWE leadership that will promote and ensure timely and high-quality, "fit-for-purpose" evidence generation.

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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