Director, Biostatistics
Locations:
Cambridge, Massachusetts, USA
Groton, Connecticut, USA
Collegeville, Pennsylvania, USA
New York City, New York, USA
Employment Type:
Full-time
Posted:
18 Days Ago
Job ID:
4937035
Our Purpose
We’re in relentless pursuit of breakthroughs that change patients’ lives. We innovate every day to make the world a healthier place.
Our Values
To fully realize Pfizer’s purpose — Breakthroughs that change patients’ lives — we have established clear expectations about what to achieve and how to achieve it.
About Pfizer Research & Development
Pfizer R&D is the heart of Pfizer's trailblazing product pipeline, driving the mission to bring life-changing medicines to the world.
Benefits
Pfizer offers competitive compensation and benefits programs designed to meet the diverse needs of our colleagues.
Job Summary
The Director of Biostatistics will lead complex global development projects in Non-Malignant Hematology within the Inflammation and Immunology & Specialty Care area. Responsibilities include clinical design oversight, trial conduct, data management, result interpretation, statistical leadership in regulatory submissions, and strategic planning. This role may involve managing contract biostatisticians and coordinating resources to ensure timely project completion.
Key Responsibilities
Provide scientific statistical input into study design, analysis plans, data interpretation, project development, and regulatory submissions.
Plan and communicate statistical analyses, data presentations, and scientific reports.
Ensure timeliness and quality of all statistical deliverables in compliance with regulatory requirements and Pfizer standards.
Collaborate effectively with clinical teams, partners, regulators, and academic organizations.
Lead cross-functional statistical activities and support planning for studies and submissions.
Participate in innovative statistical methodology research relevant to Pfizer’s business.
Basic Qualifications
Master’s in Statistics/Biostatistics (or related field) with 10+ years of clinical trials experience, OR
PhD in Statistics/Biostatistics (or related field) with 7+ years of clinical trials experience.
Experience in clinical, regulatory, and marketing operations related to clinical trials.
Proven leadership in cross-functional teams at protocol and project levels.
Strong statistical skills applied to clinical trials.
Excellent verbal and written communication.
Ability to provide oversight on clinical projects.
Proficiency in R, SAS, or Python, and experience with reproducible research tools (e.g., R Markdown, Quarto, Git/GitHub).
Leadership skills including influencing peers, coaching, and guiding teams to business impact.
Organizational Relationships
Collaborate with Clinical, Clinical Pharmacology, Statistical Programming, Data Management, Regulatory Strategy, Medical, Outcomes Research, Commercial, Operations, and external partners.
Work Location
Hybrid work model.
Compensation & Benefits
Annual base salary range: $169,700 - $282,900
Eligible for Pfizer’s Global Performance Plan with a 20% bonus target.
Eligible for share-based long-term incentives.
Comprehensive benefits including 401(k) with matching contributions, paid leave, health coverage (medical, dental, vision), and more.
Additional Information
Relocation assistance may be available based on eligibility.
Compliance with federal transparency laws (Sunshine Act).
Pfizer is an Equal Opportunity Employer.
Requires permanent U.S. work authorization.
Accessibility accommodations available upon request at disabilityrecruitment@pfizer.com.
Apply Now
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