Manager Biostatistics

A growing and recognised biopharmaceutical company is seeking a Senior Manager, Biostatistics to support an expanding portfolio of innovative clinical development programmes.

This role offers an opportunity to work within a highly scientific development environment where quantitative expertise plays an important role in advancing therapies through all stages of development. The successful candidate will contribute to the analysis, interpretation, and communication of clinical trial results while partnering closely with colleagues across the broader organisation.

The company continues to invest significantly in its late-stage pipeline and global development capabilities, offering strong visibility, career growth, and exposure to complex development challenges.

• Lead and support statistical analyses for ongoing clinical studies
• Develop, validate, and maintain Tables, Figures, and Listings (TFLs)
• Support planned and ad hoc analyses to inform study and programme decisions
• Contribute to the preparation of clinical study reports, submissions, regulatory responses, and presentations
• Collaborate with Clinical Development, Medical Affairs, Data Management, Statistical Programming, and Regulatory teams
• Support interim analyses, data reviews, and key study milestones
• Assist with analysis dataset specifications and study documentation
• Ensure timely delivery of high-quality statistical outputs aligned with regulatory and internal expectations
• Contribute to process improvement initiatives and analytical best practices
• Support data interpretation and communication of study findings to internal stakeholders

• Master's degree or PhD in Biostatistics, Statistics, Mathematics, Data Science, or a related quantitative discipline
• Experience working within pharmaceutical, biotechnology, or CRO clinical development environments
• Strong understanding of clinical trial methodology and statistical principles
• Experience supporting clinical studies through analysis and reporting activities
• Hands-on experience producing and reviewing Tables, Figures, and Listings (TFLs)
• Familiarity with SDTM and ADaM data standards
• Strong SAS and R programming skills for clinical analysis and reporting
• Experience collaborating within multidisciplinary study teams
• Ability to manage multiple priorities and work effectively in a fast-paced environment
• Strong communication and stakeholder engagement skills
• Oncology experience is highly desirable

Join a company with a broad and expanding global development pipeline

Opportunity to contribute across studies spanning early and late-stage development

Exposure to novel therapies and scientifically complex programmes

Strong collaboration with global biometrics, clinical, medical, and regulatory teams

High visibility within a growing development organisation

Competitive compensation package, bonus, equity, and long-term career progression

Chance to make a meaningful impact on therapies being developed for patients with significant unmet medical needs