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Manager, Biostatistics
PfizerBiostatistics Manager designing and executing biostatistical components for R&D projects at Pfizer. Collaborating with scientists and ensuring compliance with statistical standards in clinical research.
Posted 6/30/2026full-timeCollegeville • Massachusetts, Pennsylvania • 🇺🇸 United StatesJuniorMid-Level💰 $106,000 - $176,600 per yearWebsite
Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates strong statistical knowledge and expertise in biostatistics, with the ability to design and execute research projects while ensuring compliance with regulatory standards. Proficient in creating computational tools for data visualization and collaborating effectively with multidisciplinary teams.
Highest-signal resume keywords
Biostatistical DesignStatistical MethodologyData Visualization ToolsRegulatory ComplianceTechnical Report Writing
ATS Keywords
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Hard Skills
General Linear ModelsMixed ModelsNon-Linear ModelsExperimental DesignVariance ComponentsBayesian MethodsQuality ControlStatistical AnalysisComputational ToolsGenomic Data Technologies
Soft Skills
Effective Team PlayerExcellent Communication SkillsMentoring
Industry Keywords
International Conference on HarmonizationPharmacopoeia MonographsRegulated Scientific Environment
About the role
Key responsibilities & impact- Design, plan, and execute biostatistical components for research and development projects.
- Provide guidance and lead/co-lead moderately complex projects, managing time and resources effectively.
- Apply skills and discipline knowledge to contribute to departmental work.
- Make decisions to resolve moderately complex problems, develop new options, and operate independently in ambiguous situations.
- Work independently on assignments, receiving instruction on unusual or complex problems.
- Review your own work, seek directional review from others, and mentor colleagues by reviewing their work.
- Exercise judgment using your knowledge and experience, potentially becoming a resource for others.
- Collaborate with various scientists in the design, analysis, and reporting of clinical experiments.
- Ensure all study and project-level statistical activities comply with regulatory requirements and Pfizer standards.
- Participate in research on statistical methodology and its applications relevant to Pfizer's business needs.
Requirements
What you’ll need- MS with 2 years of relevant experience or PhD with 0+ years of relevant experience
- Strong statistical knowledge through coursework or practical application in general linear models, mixed models, non-linear models, experimental design, variance components, Bayesian methods, and quality control
- Proven ability to create computational tools for data visualization and work with modern multi-dimensional genomic data technologies
- Effective team player with excellent communication skills and the ability to write technical reports
- Familiarity with International Conference on Harmonization guidance and pharmacopoeia monographs
- Experience in a regulated scientific environment, demonstrating statistical expertise
- Ability to prepare both internal and external reports, presentations, and manuscripts
Benefits
Comp & perks- 401(k) plan with Pfizer Matching Contributions
- Additional Pfizer Retirement Savings Contribution
- Paid vacation
- Holiday and personal days
- Paid caregiver/parental and medical leave
- Health benefits to include medical, prescription drug, dental and vision coverage