Work with senior level statistician to provide statistically sound experimental design and data analysis strategies
Contribute to the development of clinical study protocols and author the statistical sections
Develop statistical analysis plans and work with programming to create table, listing and figure shells
Independently derive from source data key efficacy variables and analyses
Perform the analyses of clinical trial data and collaborate on the reporting of clinical trial results to the scientific community
Participate in the development and maintenance of department tools, templates, and guidelines

Requirements

Master’s degree in Statistics or Biostatistics with minimum 2 years of experience in an applied statistics setting, or a Ph.D. in Statistics, Biostatistics, or a comparable quantitative field
Ability to learn/gain working knowledge of FDA/EMA or other regulations
ICH GCP guidelines
Drug development process
CDISC standards and implementation guides
Company SOPs and business practices
Proficient in statistical methods and applications to clinical trial design and data analysis
Programming skills in R and/or SAS

Benefits

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 including medical, prescription drug, dental and vision coverage

Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills & Tools

statistical analysisexperimental designdata analysis strategiesstatistical analysis plansprogramming in Rprogramming in SASclinical trial designstatistical methodsefficacy variablesdata reporting

Certifications

Master’s degree in StatisticsMaster’s degree in BiostatisticsPh.D. in StatisticsPh.D. in Biostatistics