Associate Director, Biostatistics

Pfizer Com Ec

Base: $139,100.00 to $231,900.00; bonus/equity: 17...
Hybrid
Clinical study design and analysis
Statistical programming in r or sas
Fda/ema regulatory knowledge
The Associate Director, Biostatistics is responsible for providing statistical leadership and expert analysis for clinical studies across various phases, contributing to study design, data interpretation, and regulatory submissions

Job Summary

  • The Associate Director, Biostatistics is responsible for providing statistical leadership and expert analysis for clinical studies across various phases, contributing to study design, data interpretation, and regulatory submissions.
  • This role offers a hybrid work location and includes a competitive salary range with bonus eligibility and comprehensive benefits such as 401(k) plans, paid leave, and health coverage.
  • Pfizer is committed to equal opportunity employment and requires permanent work authorization in the United States with no visa sponsorship available for this position.

Matching Summary

The Associate Director, Biostatistics is responsible for providing statistical leadership and expert analysis for clinical studies across various phases, contributing to study design, data interpretation, and regulatory submissions.

Salary

Base: $139,100.00 to $231,900.00; Bonus/Equity: 17.5% bonus target and share-based long term incentives; Benefits: 401(k) with matching, paid leave, health coverage

Skills & Requirements

Must-have

  • Clinical study design and analysis
  • Statistical programming in R or SAS
  • FDA/EMA regulatory knowledge
  • ICH GCP guideline compliance
  • CDISC standards implementation
  • Statistical input for clinical protocols
  • Clinical trial data interpretation

Nice-to-have

  • Oncology experience
  • Statistical research and simulation skills
  • Cross-functional collaboration
  • Multi-mode communication skills
  • Leadership and coaching capabilities
  • Project management
  • Adaptability and problem solving

Key Requirements

  • Ph.D. in Statistics or related field with 5+ years experience
  • Master’s degree with 7+ years clinical trial experience
  • Permanent US work authorization
  • Experience with FDA/EMA regulations
  • Knowledge of ICH GCP guidelines
  • Proficiency in R and/or SAS programming

Work Rights

Permanent US work authorization required

Tailored Resume

Cover Letter