Recruitment Data Policies Senior RWE (Real World Evidence) Expert

Make your mark for patients

We are looking for a Senior Real-World Evidence (RWE) Expert who is scientifically rigorous strategically minded and passionate about generating impactful evidence. You will join our Global Real-World Evidence team working both with US and non-US colleagues. This is a hybrid position and could be either based out of our offices in Cambridge MA or Raleigh NC or Atlanta GA.

As a Senior Real-World Evidence Expert you will independently design lead and deliver global evidence studies. Your work will inform internal decisions support regulatory and payer interactions and advance scientific understanding of disease areas. You will also help shape asset-level evidence strategies and propose innovative approaches in partnership with the Real-World Evidence Strategy Lead.

You will collaborate with statisticians analysts epidemiologists clinical teams market access and health economics colleagues safety and pharmacovigilance partners medical experts external vendors and cross-functional asset teams. As an influential scientific contributor you will align diverse stakeholders and ensure outputs meet strategic regulatory payer and scientific needs.

• Lead complex global evidence studies using diverse methodologies data sources and study designs.
• Develop study concepts protocols analysis plans governance processes and quality-control standards.
• Deliver epidemiology disease-burden safety regulatory and comparative-effectiveness studies.
• Lead primary data-collection partnerships and high-visibility secondary data-use initiatives.
• Interpret and communicate findings across scientific regulatory payer and strategic forums.
• Shape asset evidence strategies through innovative methods data sources and functional thought leadership.

• Masters PhD PharmD or MD in a relevant scientific or quantitative field.
• 8 years of experience designing and delivering real-world evidence studies in industry or consulting. (Experience from academia may also be considered).
• Strong expertise in RWE methodology including epidemiology pharmacoepidemiology outcomes research and quantitative methods.
• Experience using a variety of real-world data sources ideally including both primary and secondary data sources with an ability to critically evaluate fitness for purpose.
• Ability to create high-quality abstracts manuscripts posters presentations and scientific communications.
• Excellent communication and influence skills with cross-functional teams and senior stakeholders.
• Independent project leadership strategic thinking innovation and adaptability in changing environments.

The reasonably anticipated base salary range for this position is $164000 to $215300 per year. The actual salary offered will take into account related knowledge skills experience and location among other factors and may fall outside the expected range.

Are you ready to go beyond to create value and make your mark for patients If this sounds like you then we would love to hear from you!

About us
UCB is a global biopharmaceutical company focusing on neurology and immunology. We are over 9.000 people in all four corners of the globe inspired by patients and driven by science.

Why work with us
At UCB we dont just complete tasks we create value. We arent afraid to push forward collaborate and innovate to make our mark for patients. We have a caring supportive culture where everyone feels included respected and has equal opportunities to do their best work. We go beyond to create value for our patients and always with a human focus whether thats on our patients our employees or our planet. Working for us you will discover a place where you can grow and have the freedom to carve your own career path to achieve your full potential.

At UCB weve embraced a hybrid-first approach to work bringing teams together in local hubs to foster collaborative curiosity. Unless explicitly stated in the description or precluded by the nature of the position roles are hybrid with 40% of your time spent in the office.

UCB is an equal opportunity 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 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.