Senior Biostatistician (UK/Europe)

Join a global Contract Resource Organization (CRO) where innovation meets purpose. At Worldwide Clinical Trials, we're driven by a shared commitment to improving lives through high-quality clinical research. Our teams are empowered to think creatively, take ownership, and deliver meaningful work that helps bring life-changing therapies to patients around the world.

With more than 4,000 professionals across the globe, we foster a collaborative and inclusive environment where diverse perspectives are valued, growth is encouraged, and every contribution makes an impact. Whether you're building your career or bringing years of experience, you'll have the opportunity to learn, grow, and help shape the future of clinical research.

Make an Impact as a Senior Biostatistician at Worldwide

As a Senior Biostatistician, you will provide expert statistical leadership across clinical projects and sponsor programmes, helping ensure that study design, analysis, and reporting activities are delivered with scientific rigour and quality. Your expertise will directly support the generation of reliable clinical evidence that informs important development decisions.

Working closely with sponsors, cross-functional teams, and external partners, you'll act as a trusted statistical consultant, contributing to study design, analysis strategies, reporting, and regulatory-compliant deliverables. You'll also play a key role in driving process improvements, supporting innovation, and enhancing the efficiency and quality of statistical operations.

This is an opportunity to combine hands-on technical expertise with strategic statistical leadership, making a meaningful impact across multiple clinical development programmes.

Where You'll Work

This is a remote role open to candidates based in UK or Europe. You will collaborate with global teams across multiple time zones.

What You'll Do

• Lead statistical support for clinical projects and sponsor programmes, ensuring high-quality and timely consultancy throughout the study lifecycle.
• Provide expert review and guidance on study designs, statistical analysis plans, protocols, and clinical study reports.
• Partner with sponsors and internal teams to develop robust statistical methodologies, randomisation strategies, and analysis approaches.
• Develop, review, validate, and maintain SAS programs for clinical data analysis, CDISC datasets (SDTM and ADaM), and statistical reporting outputs.
• Deliver statistical reporting activities, including specifications for tables, figures, listings, derived datasets, and final study deliverables.
• Collaborate with internal departments, sponsors, and external stakeholders to address statistical issues and reporting requirements.
• Drive process and system improvements that enhance the quality, efficiency, and consistency of clinical study data processing and reporting.
• Contribute to publications, presentations, bid support activities, statistical policies, quality initiatives, and audit readiness efforts.

What You'll Bring

• Degree in Mathematics, Statistics, or another discipline with a strong statistical component.
• Extensive hands-on experience as a project biostatistician, providing statistical leadership across clinical research projects.
• Strong expertise in clinical trial design, statistical analysis, reporting methodologies, and statistical consultancy.
• Advanced SAS programming skills, including experience with derived datasets, CDISC SDTM and ADaM standards, tables, figures, and listings.
• Knowledge of relevant regulatory guidance and industry standards, including ICH requirements, FDA Quality System Regulation (21 CFR Part 11), and related clinical research regulations.
• Experience reviewing and producing statistical analysis plans, study reports, and publication-quality outputs.
• Strong stakeholder management, communication, relationship-building, and influencing skills.
• Proficiency in English.

Discover the Difference

We love knowing that someone is going to have a better life because of the work we do.  Discover the Difference at Worldwide Clinical Trials. Explore additional opportunities on our careers page, visit http://www.worldwide.com/careers, or connect with us on LinkedIn.

About Us

This is who we are.

We’re a team of clinicians, scientists, and researchers who want to make healthcare better. We were founded on an unwavering commitment to authentic, personalized attention. And today, as CROs consolidate and the industry changes rapidly, that personalized attention is more important than ever.

We all came to this industry for different reasons, from different walks of life. If you ask any one of us why we’re here, you’ll get a different answer. And that’s what makes us special.