Statistical Methodologist, Raleigh, NC

Statistical Methodologist

Make your mark for patients

We are looking for a Statistical Methodologist who is innovative, collaborative, and analytically rigorous to join us in our Biometrics and Data Science team, based in our Atlanta, GA headquarters.

About the role

As a Statistical Methodologist, you will provide expert statistical consultation across the drug development lifecycle, from early clinical development through late-stage and lifecycle activities. You will help design, analyze, and optimize innovative clinical studies, contribute to the development of advanced statistical methodologies, and translate complex quantitative evidence into clear, decision-relevant insights that impact clinical, regulatory, and commercial strategies.

Who you'll work with

You will be part of the Statistical Innovation group within Biometrics and Data Science, collaborating closely with cross-functional partners including clinical, regulatory, data science, and medical colleagues. The team operates globally and engages both internally and externally through scientific collaborations, industry working groups, and conference participation.

What you'll do

• Provide statistical methodology support across clinical trials and development stages.
• Design and assess innovative clinical trial methods and analytical approaches.
• Apply frequentist and Bayesian methods to complex drug development questions.
• Conduct simulations to inform study design, sample size, and power decisions.
• Communicate complex statistical concepts using clear visuals and narratives.
• Contribute to publications, presentations, and cross-industry scientific initiatives.

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

Minimum Qualifications

• PhD in statistics, mathematics, or related quantitative discipline.

Preferred Qualifications

• Strong experience with advanced statistical methodologies in drug development.
• Proficiency in statistical programming, including R and/or SAS.
• Knowledge of global regulatory frameworks, including FDA and EMA guidance.
• Ability to communicate complex statistics to technical and nontechnical audiences.

• Experience applying Bayesian methods and innovative trial designs.
• Record of methodological publications or conference presentations.
• Experience working in a global, cross-functional pharmaceutical environment.

This position's reasonably anticipated salary range is $88k-$115k per year. The actual salary offered will take into account internal equity and also may vary depending on the candidate's geographic region, job-related knowledge, skills, and experience, among other factors.

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 don't just complete tasks, we create value. We aren't 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 that's 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, we've 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 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-Rea 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.