Senior Biostatistics Lead - Clinical Development

Bristol-Myers Squibb Co; Uxbridge; Hybrid; GBP 90,000 - 120,000; Full time

Job summary

Bristol Myers Squibb in Uxbridge is seeking an Associate Director of Biostatistics to join cross-functional development teams. You will contribute to trial design, analysis planning, and regulatory submissions, with half of the time onsite.

The role requires a PhD (6+ yrs) or MSc (8+ yrs) in statistics/biostatistics with clinical trials experience, plus strong SAS/R/Python skills and excellent communication and leadership abilities. Hybrid work model offers flexibility and impact across programs.

Qualifications

• PhD (6+ years’ experience) or MSc (8+ years’ experience) in statistics/biostatistics or related field with clinical trials experience.
• Proficiency in SAS, R or Python with advanced analysis, data manipulation and simulation.
• Excellent interpersonal, written and organizational skills.
• Expertise in statistical/clinical trials methodology for clinical development and regulatory interactions.

Responsibilities

• Collaborates in design of innovative clinical trials and endpoints to address study objectives.
• Defends protocols and analysis plans in governance reviews.
• Authors or reviews protocols, SAPs, CSRs and other study documents.
• Presents data and analyses clearly and transparently to stakeholders.
• Provides statistical support for regulatory interactions and health authority requests.
• Manages multiple studies ensuring consistency and quality of deliverables within a therapeutic area.
• Engages as a matrix team member as a scientific and strategic partner in drug development.

Skills

Biostatistics

Team leadership

SAS

R

Education

PhD

MSc

Tools

SAS

R

Python

Job description

Bristol Myers Squibb in Uxbridge is seeking an Associate Director of Biostatistics to join cross-functional development teams. You will contribute to trial design, analysis planning, and regulatory submissions, with half of the time onsite.

The role requires a PhD (6+ yrs) or MSc (8+ yrs) in statistics/biostatistics with clinical trials experience, plus strong SAS/R/Python skills and excellent communication and leadership abilities. Hybrid work model offers flexibility and impact across programs.