Associate Director, Biostatistics

pfizer.hu

Base: $139,100 to $231,900; bonus/equity: 17.5% bo...
Hybrid
Clinical study design expertise
Statistical analysis of clinical trials
Knowledge of fda/ema regulations
The Associate Director, Biostatistics serves as a study statistician for clinical studies and provides statistically sound experimental design and data analysis strategies to meet project objectives

Job Summary

  • The Associate Director, Biostatistics serves as a study statistician for clinical studies and provides statistically sound experimental design and data analysis strategies to meet project objectives.
  • This role offers a competitive salary range with bonus and long-term incentive programs, as well as comprehensive benefits including retirement plans, paid leave, and health coverage.
  • Pfizer is committed to equal opportunity employment and requires permanent work authorization in the United States without visa sponsorship.

Matching Summary

The Associate Director, Biostatistics serves as a study statistician for clinical studies and provides statistically sound experimental design and data analysis strategies to meet project objectives.

Salary

Base: $139,100 to $231,900; Bonus/Equity: 17.5% bonus target plus share-based long term incentives; Benefits: 401(k) with matching, paid leave, medical and other health coverage

Skills & Requirements

Must-have

  • clinical study design expertise
  • statistical analysis of clinical trials
  • knowledge of FDA/EMA regulations
  • programming skills in R and SAS
  • development of statistical analysis plans
  • experience with CDISC standards

Nice-to-have

  • strong communication skills
  • ability to manage multiple projects
  • leadership and collaboration capabilities
  • adaptability to shifting demands
  • oncology experience
  • statistical research and simulation skills

Key Requirements

  • Ph.D. in Statistics or related field with 5+ years experience
  • Master’s degree with 7+ years clinical trials experience
  • permanent U.S. work authorization
  • knowledge of ICH GCP guidelines
  • experience with clinical trial sample size calculations

Work Rights

Permanent U.S. work authorization required

Tailored Resume

Cover Letter