Provide scientifically rigorous statistical input into clinical development plans, protocol development, statistical analysis plans, regulatory submissions and responses, and other product support initiatives.
Be accountable for study- and program-level statistical deliverables, ensuring timeliness and quality in accordance with project plans.
Coordinate statistical support activities under appropriate business models (e.g., FSPs), including resource allocation and progress monitoring.
Develop effective collaborations with clinical teams and partner lines (e.g., Development Operations, Safety Risk Management, Regulatory).
Ensure all statistical activities comply with relevant regulatory requirements and Pfizer standards.
Plan, deliver, and communicate statistical analyses, data presentations, and scientific reports.
Identify opportunities to apply innovative statistical methodologies to streamline clinical development and support optimal decision-making.
Participate in research on statistical methodologies relevant to Pfizer’s business needs.
Help maintain a strong statistics community at Pfizer through collaboration, knowledge sharing, presentations, and process improvement initiatives.
Requirements
M.S. in Statistics, Biostatistics, or a related field with a minimum of 5 years of applied statistical experience; or Ph.D. in Statistics, Biostatistics, or a related field with a minimum of 1 year of experience.
Effective verbal and written communication skills, including the ability to engage with colleagues, stakeholders, and regulatory authorities.
Demonstrated capability to provide statistical leadership within cross-functional teams.
Candidate demonstrates a breadth of diverse leadership experiences and capabilities including: the ability to influence and collaborate with peers, develop and coach others, oversee and guide the work of other colleagues to achieve meaningful outcomes and create business impact.
Relevant experience in the design, implementation, analysis, and reporting of clinical trials, particularly in vaccine development (preferred).
Proven track record of applying advanced statistical methods to clinical trials and regulatory submissions (preferred).
Experience working with outsourcing partners or CROs (preferred).
Knowledge and application of statistical modeling, simulation, meta-analysis, and other advanced methodologies using diverse data sources (preferred).
Business experience that provides an understanding of clinical, regulatory, and marketing operations (preferred).
Permanent work authorization in the United States required.
Benefits
Participation in Pfizer’s Global Performance Plan with a bonus target of 17.5% of the base salary
Eligibility to participate in Pfizer’s share based long term incentive program
401(k) plan with Pfizer Matching Contributions and an additional Pfizer Retirement Savings Contribution
Paid vacation, holiday and personal days
Paid caregiver/parental and medical leave
Health benefits including medical, prescription drug, dental and vision coverage
Comprehensive and generous benefits and programs to support colleagues’ lives
Relocation support/assistance may be available based on business needs and/or eligibility
Applicant Tracking System Keywords
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