- 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
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Director, Biostatistics employer: Jobtailor
As a Client Services Coordinator at our dynamic company, you will thrive in a supportive work culture that prioritises employee growth and development. We offer comprehensive training, opportunities for advancement, and a collaborative environment where your contributions are valued. Located in a vibrant area, our team enjoys a healthy work-life balance and the chance to engage with diverse clients, making every day rewarding and meaningful.
