Manager, Biostatistics

Jobtailor; Massachusetts; On-site; USD 110,000 - 170,000; Full time

Job summary

Pfizer seeks a biostatistician to design, plan, and execute statistical components for R&D projects. You will apply advanced modeling techniques and collaborate with scientists to drive analyses from design through reporting.

You will mentor colleagues, review work, and ensure study activities meet regulatory requirements and Pfizer standards. The role requires clear communication of methods and results in internal and external reports.

Qualifications

• 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.

Responsibilities

• Design, plan, and execute biostatistical components for R&D 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.

Skills

Biostatistics

Statistical modeling

Data visualization

Report writing

Team collaboration

Education

MS in Biostatistics

PhD in Biostatistics

Tools

Genomic data tools

Job description

Responsibilities

• 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.

Qualifications

• 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.