RWE Senior Expert - Special Patient Populations

Make your mark for patients

We are looking for a RWE Senior Expert - Special Patient Populations who is collaborative, solutions-oriented, and passionate about leveraging real world data to improve the patient experience to join our Global Real World Evidence Team. This role can based in Cambridge, Massachusetts, Raleigh, North Carolina, or in Atlanta, Georgia. This hybrid role requires a minimum of 40% on-site presence and 5-10% domestic and international travel.

About the Role

You will lead the design and execution of global real-world evidence programs that generate insights to support research and development, guide strategic business decisions, advance understanding of disease and patient outcomes, and fulfill post-market requirements. Your work will help inform decision-making for a wide range of stakeholders, including patients, healthcare professionals, regulators, policymakers, and payers. A key focus of this role is generating evidence and developing real-world data capabilities for special patient populations, including women of childbearing age, pediatric patients, and older adults, to address critical clinical, regulatory, and healthcare decision-making needs.

You will be responsible for developing and strengthening real-world data capabilities across specific disease areas, with a particular focus on women of childbearing age and other specialized patient populations, including pediatric and elderly patients. Working closely with cross-functional partners, you will also shape and deliver the overarching real-world evidence strategy for key development and commercial assets.

Who you'll work with

Internally, you will work closely with colleagues across Clinical Development, Medical Affairs, Drug Safety and Pharmacovigilance, Regulatory Affairs, Health Economics and Outcomes Research, Market Access, Biostatistics, Data Science, Evidence Generation, and Asset Strategy teams to develop and deliver evidence strategies that support decisions across the product lifecycle.

Externally, you will partner with academic researchers, healthcare providers, key opinion leaders, healthcare data partners, contract research organizations, and regulatory stakeholders to generate high-quality evidence, advance scientific understanding, and address critical clinical, regulatory, and market access questions.

What you'll do

• Lead the design and execution of global real-world evidence studies that support research, development, regulatory, medical, market access, and business decision-making.
• Develop evidence-generation strategies for special patient populations, including individuals who are pregnant, pediatric populations, older adults, and other underrepresented patient groups.
• Deliver complex observational research programs using real-world data and prospective data collection, ensuring scientific rigor, operational excellence, and timely execution.
• Partner with cross-functional teams to identify evidence needs related to disease burden, treatment outcomes, safety, effectiveness, and patient care pathways across the product lifecycle.
• Translate study findings into actionable insights and communicate results to internal stakeholders, external partners, scientific audiences, and regulatory bodies.
• Collaborate with external experts, research partners, and healthcare data providers to advance innovative evidence-generation approaches.
• Shape long-term evidence strategies for priority assets and disease areas while identifying opportunities to leverage new data sources, advanced analytics, machine learning, and artificial intelligence.
• Serve as a trusted scientific advisor, championing robust methodologies and evidence-based decision-making across the organization.

Interested? For this role we're looking for the following education, experience and skills

Minimum Experience/Skills Required:

• Advanced degree in Life Sciences, Epidemiology, Health Economics, Biostatistics, Data Science, Public Health, or a related field.
• At least 6 years of experience designing, leading, and delivering real-world evidence studies in the pharmaceutical, biotechnology, consulting, or academic sectors.
• Demonstrated experience using primary and secondary healthcare data to generate evidence that informs clinical, regulatory, medical, or commercial decision-making.
• Strong expertise in epidemiology, outcomes research, observational study design, and quantitative research methods.
• Experience working across global or regional cross-functional teams and managing complex research initiatives from concept through execution.
• Excellent written and verbal communication skills with the ability to present complex findings to diverse audiences.

Preferred Qualifications

• Doctoral degree in Epidemiology, Outcomes Research, Public Health, Statistics, or a related scientific discipline.
• Experience supporting evidence-generation strategies across the product lifecycle, including regulatory, medical affairs, market access, and health technology assessment needs.
• Experience in maternal health, pregnancy, lactation, fertility, neonatal health, pediatric populations, older adult populations, or other special patient populations.
• Proven track record of developing scientific publications, abstracts, posters, presentations, and peer-reviewed manuscripts.
• Experience with innovative real-world evidence study designs, external control arms, comparative effectiveness research, and post-authorization safety or effectiveness studies.
• Interest in applying advanced analytics, machine learning, and artificial intelligence to real-world data and evidence-generation activities.
• Demonstrated ability to influence stakeholders and translate complex evidence into actionable business and scientific recommendations.

Internal applicants should be in their current job for at least 12 months, must meet performance standards and are not on formal corrective/disciplinary process (PIP), warning, final warning, or compliance warning letters within the last 12 months. Please inform your Manager or your Talent Partner before applying to any internal job opportunities.

Unless explicitly stated in the description, this role is hybrid with 40% of your time spent in the office, regardless of your current contractual agreement. If your current working arrangements differ, please contact your Talent Partner to discuss before submitting your application.

UCB is an equal opportunity employer. All employment decisions will be made without regard to any characteristic protected by applicable federal, state, or local law. UCB invites you to voluntarily self-identify during the application process. Provision of self-identification information is entirely voluntary and a decision to provide or not provide such information will not have any effect on your application for employment, your employment with UCB, or otherwise subject you to any adverse treatment. Any information you provide will be considered confidential and will be kept separate from your application and/or personnel file and will only be used in accordance with applicable laws, orders, and regulations.

Should you require any adjustments to our process to assist you in demonstrating your strengths and capabilities contact us on US-Reasonable_Accommodation@ucb.com for application to US based roles. Please note should your enquiry not relate to adjustments; we will not be able to support you through this channel.

Requisition ID: 93925

Recruiter: Parth Suthar

Hiring Manager: Lesley Butler

Talent Partner: Bénédicte Demoulin

Job Level: MM I

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