Senior Project Lead Statistician for Early Development

Ucb; Slough; Vor Ort; GBP 90.000 - 120.000; Vollzeit

Zusammenfassung

UCB is seeking a Project Lead Statistician to set the strategic direction for statistics across therapeutics and compound programs, shaping early development with innovative study designs and quantitative decision-making. You will join the Development Team and influence cross-functional partners to deliver robust analyses.

The role requires leading global teams, driving analytics, and contributing to regulatory submissions.

Qualifikationen

• PhD preferred in Biostatistics or Statistics with 10+ years in pharma; a Master's with 12+ years is also considered.
• Experience leading global teams and designing, analyzing and reporting clinical trials across all phases.
• Experience applying innovative statistical approaches and quantitative decision-making under uncertainty.
• Experience supporting or managing submissions to global health authorities (FDA/EMA/etc.).
• Proficiency in SAS or R and sample size/simulation software; CDISC SDTM/ADaM and PK/PD experience desired.
• Ability to influence, navigate ambiguity and explain complex statistical ideas clearly, with excellent English.

Aufgaben

• Set your statistics team's strategy and be accountable for its deliverables.
• Guide and influence overall strategy for your compounds with Development and Regulatory leads.
• Share strategic input on quantitative innovation, analytics, program design and digital transformation.
• Help transform the statistics operating model and implement UCB Data Strategy.
• Manage people, set objectives, guide careers and encourage mentoring and continuous learning.
• Represent UCB internally and externally and plan resources, budgets and travel.

Kenntnisse

Leadership

Strategic thinking

Communication

Team collaboration

Ausbildung

PhD in Biostatistics

Masters in Biostatistics

Tools

SAS

R

CDISC SDTM/ADaM

PK/PD software

Jobbeschreibung

UCB is seeking a Project Lead Statistician to set the strategic direction for statistics across therapeutics and compound programs, shaping early development with innovative study designs and quantitative decision-making. You will join the Development Team and influence cross-functional partners to deliver robust analyses.

The role requires leading global teams, driving analytics, and contributing to regulatory submissions.