Director, Biostatistics

Plan, direct, and coordinate specialized and complex global development projects in Inflammation and Immunology & Specialty Care Oversee clinical design, trial conduct, data management, result interpretation, and statistical support for global regulatory submissions Implement new initiatives and assist in strategic planning Manage contract biostatisticians when required, including resource allocation, work assignment scheduling, and project status monitoring Provide statistical input to study design, statistical analysis plans, interpretation of results, development plans, regulatory issues, and registration projects Plan and communicate statistical analyses, data presentations, and scientific reports Support publication activities, scientific presentations, and product defense Ensure timely and high-quality study and submission statistical deliverables Ensure statistics activities comply with regulatory requirements and Pfizer standards Collaborate with clinical teams, partner functions

external regulatory, industry, professional, and academic organizations Provide statistical leadership to cross-functional activities, assigned studies, and regulatory submissions Provide planning input to the Statistics Group Lead Participate in research on innovative statistical methodology and applications Requirements Masters in Statistics/Biostatistics (or related field) with extensive experience in clinical trials, or PhD in Statistics/Biostatistics (or related field) with notable experience in clinical trials Relevant clinical trial and business experience understanding clinical, regulatory and marketing operations Capability to provide statistical leadership to cross-functional teams at protocol and project level Strong statistical skills applied to clinical trials Effective verbal and written communication skills Experience providing statistical support and oversight for one or more clinical projects Ability to perform mathematical and statistical calculations Ability to perform
complex data analysis Proficiency in R, SAS, or Python Experience with at least one reproducible research tool, such as R Markdown, Quarto, or Git/GitHub All applicants must have relevant authorisation to live and work in the UK Core Competencies Demonstrates expertise in statistical analysis and clinical trial design, providing leadership in cross-functional teams and ensuring compliance with regulatory standards. Proficient in statistical programming and data analysis, with a strong focus on delivering high-quality results for global regulatory submissions. Highest-signal resume keywords Masters In Statistics/Biostatistics PhD In Statistics/Biostatistics Statistical Leadership Proficiency In R, SAS, Or Python Clinical Trial Experience ATS Optimization Keywords Hard Skills Statistical Analysis Data Management Complex Data Analysis Statistical Calculations Statistical Support Study Design Statistical Analysis Plans Regulatory Submissions Publication Activities Scientific Presentations
Soft Skills Effective Communication Skills Industry Keywords Clinical Trials Regulatory Requirements Inflammation Immunology Specialty Care Tools & Technologies R Markdown Quarto Git/GitHub #J-18808-Ljbffr