Senior Real World Evidence Expert Bimzelx (Germany)
Job Description
Make your mark for patients
We are looking for aSenior Real World Evidence Expertwho is scientifically rigorous, strategically minded, and collaborative to join ourReal‑World Evidence (RWE) team, helping to shape evidence generation strategies that support better decisions for patients, healthcare systems, and the broader scientific community. This position can bebased in Brussels, Belgium; Slough, UK; Monheim, Germany or Atlanta, USA.
About the Role
As Senior RWE Expert, you will be responsible for designing and delivering global real‑world evidence (RWE) studies that generate impactful insights across the product lifecycle.
You will contribute to strategic decision‑making by developing evidence that supports research and development activities, regulatory requirements, payer needs, and clinical practice.
In this role, you will help drive the development of asset‑level RWE strategies, working closely with cross‑functional stakeholders to identify evidence gaps, generate meaningful insights, and advance innovative approaches to evidence generation. You will also contribute to the evolution of real‑world data capabilities and methodologies that strengthen UCB’s ability to address complex healthcare challenges.
Who You’ll Work With
You will work closely with RWE Strategy Leads, Epidemiology and Evidence Synthesis teams, Safety and Pharmacovigilance colleagues, Biostatisticians, Data Scientists, and external research partners.
You will collaborate across global functions to ensure evidence generation activities are aligned with strategic priorities and deliver meaningful value to patients and stakeholders.
What You’ll Do
- Lead the design, execution, and delivery of complex global RWE studies on time and within budget.
- Develop study concepts, protocols, statistical analysis plans, and study documentation to support evidence generation objectives.
- Drive epidemiology, natural history, disease burden, comparative effectiveness, safety, and post‑launch evidence generation initiatives.
- Lead secondary data studies and represent RWE in primary data collection study teams.
- Collaborate with external vendors, academic researchers, and medical experts to ensure high‑quality study execution.
- Interpret and communicate study findings to both internal and external stakeholders.
- Support the development and execution of asset‑level RWE strategies and evidence plans.
- Identify and implement innovative study designs, advanced analytics methodologies, and new real‑world data sources.
- Contribute to scientific publications, abstracts, posters, presentations, and external communications.
- Act as a trusted subject matter expert, providing strategic guidance and championing scientifically robust methodologies.
Interested? For this role we’re looking for:
- Master’s degree, PhD, MD, or equivalent qualification in epidemiology, outcomes research, health economics, biostatistics, life sciences, or a related discipline.
- Significant experience designing and delivering real‑world evidence studies using primary and/or secondary data sources.
- Strong expertise in epidemiology, pharmacoepidemiology, outcomes research, health economics, biostatistics, data science, or related quantitative disciplines.
- Experience working within pharmaceutical, biotechnology, consulting, or academic research environments.
- Excellent communication skills with the ability to translate complex evidence into clear and actionable insights.
- Passion for innovation, scientific excellence, and the application of emerging technologies, including AI‑enabled approaches within real‑world evidence generation.
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.
At UCB, we’ve embraced a hybrid-first approach to work, bringing teams together in local hubs to foster collaborative curiosity. Unless expressly stated in the description, this role is hybrid with 40% of your time spent in the office, irrespective of your current contractual agreement. Should your current working arrangements differ, please contact your Talent Partner to discuss, before submitting your application.
Make your mark for patients
We are looking for aSenior Real World Evidence Expertwho is scientifically rigorous, strategically minded, and collaborative to join ourReal‑World Evidence (RWE) team, helping to shape evidence generation strategies that support better decisions for patients, healthcare systems, and the broader scientific community. This position can bebased in Brussels, Belgium; Slough, UK; Monheim, Germany or Atlanta, USA.
About the Role
As Senior RWE Expert, you will be responsible for designing and delivering global real‑world evidence (RWE) studies that generate impactful insights across the product lifecycle.
You will contribute to strategic decision‑making by developing evidence that supports research and development activities, regulatory requirements, payer needs, and clinical practice.
In this role, you will help drive the development of asset‑level RWE strategies, working closely with cross‑functional stakeholders to identify evidence gaps, generate meaningful insights, and advance innovative approaches to evidence generation. You will also contribute to the evolution of real‑world data capabilities and methodologies that strengthen UCB’s ability to address complex healthcare challenges.
Who You’ll Work With
You will work closely with RWE Strategy Leads, Epidemiology and Evidence Synthesis teams, Safety and Pharmacovigilance colleagues, Biostatisticians, Data Scientists, and external research partners.
You will collaborate across global functions to ensure evidence generation activities are aligned with strategic priorities and deliver meaningful value to patients and stakeholders.
What You’ll Do
- Lead the design, execution, and delivery of complex global RWE studies on time and within budget.
- Develop study concepts, protocols, statistical analysis plans, and study documentation to support evidence generation objectives.
- Drive epidemiology, natural history, disease burden, comparative effectiveness, safety, and post‑launch evidence generation initiatives.
- Lead secondary data studies and represent RWE in primary data collection study teams.
- Collaborate with external vendors, academic researchers, and medical experts to ensure high‑quality study execution.
- Interpret and communicate study findings to both internal and external stakeholders.
- Support the development and execution of asset‑level RWE strategies and evidence plans.
- Identify and implement innovative study designs, advanced analytics methodologies, and new real‑world data sources.
- Contribute to scientific publications, abstracts, posters, presentations, and external communications.
- Act as a trusted subject matter expert, providing strategic guidance and championing scientifically robust methodologies.
Interested? For this role we’re looking for:
- Master’s degree, PhD, MD, or equivalent qualification in epidemiology, outcomes research, health economics, biostatistics, life sciences, or a related discipline.
- Significant experience designing and delivering real‑world evidence studies using primary and/or secondary data sources.
- Strong expertise in epidemiology, pharmacoepidemiology, outcomes research, health economics, biostatistics, data science, or related quantitative disciplines.
- Experience working within pharmaceutical, biotechnology, consulting, or academic research environments.
- Excellent communication skills with the ability to translate complex evidence into clear and actionable insights.
- Passion for innovation, scientific excellence, and the application of emerging technologies, including AI‑enabled approaches within real‑world evidence generation.
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.
At UCB, we’ve embraced a hybrid-first approach to work, bringing teams together in local hubs to foster collaborative curiosity. Unless expressly stated in the description, this role is hybrid with 40% of your time spent in the office, irrespective of your current contractual agreement. Should 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 laws.
Should you require any adjustments to our process to assist you in demonstrating your strengths and capabilities contact us on EMEA-Reasonable_Accommodation@ucb.com . Please note should your enquiry not relate to adjustments; we will not be able to support you through this channel.
Requisition ID:93915
Recruiter:Gavin Savage
Hiring Manager:Aijing Shang
Talent Partner:Bénédicte Demoulin
Job Level:MM I
Please consult HRAnswers for more information on job levels.
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