Scientific Associate Director - Toxicology

Bristol Myers Squibb

New Brunswick, NJ, US
Base: $178,690 - $249,003 depending on location; b...
50% onsite
15+ years academic or industry experience
6+ years leadership experience
Glp/nonglp study oversight
The role involves overseeing nonclinical safety evaluation programs for selected drug candidates across oncology, hematology, and other therapeutic areas

Job Summary

  • The role involves overseeing nonclinical safety evaluation programs for selected drug candidates across oncology, hematology, and other therapeutic areas.
  • Candidates will write and critically review submission documents such as CTD sections for INDs and NDAs while interacting with global regulatory agencies.
  • Bristol Myers Squibb offers a wide variety of competitive benefits including health coverage, financial protection, and flexible time off policies.

Matching Summary

The role involves overseeing nonclinical safety evaluation programs for selected drug candidates across oncology, hematology, and other therapeutic areas.

Salary

Base: $178,690 - $249,003 depending on location; Bonus/Equity: Additional incentive cash and stock opportunities available; Benefits: Health, dental, vision, 401(k), paid time off, and wellness programs

Skills & Requirements

Must-have

  • 15+ years academic or industry experience
  • 6+ years leadership experience
  • GLP/nonGLP study oversight
  • CTD section writing for INDs and NDAs
  • Regulatory agency interaction

Nice-to-have

  • Knowledge of immunology and pharmacology
  • Experience with in vitro and in vivo mechanisms
  • Strong written and oral communication skills
  • Ability to manage multiple research activities
  • Collaborative team spirit

Key Requirements

  • Bachelor's Degree with 15+ years experience
  • Master's Degree with 12+ years experience
  • PhD with 8+ years experience
  • 6+ years of leadership experience
  • US work authorization required

Work Rights

Not specified

Tailored Resume

Cover Letter