Brisbane - ca - us: $205,490 - $249,003; cambridge...
50% onsite
Nonclinical safety evaluation programs
Design and reporting of toxicity studies
Regulatory agency interaction
Nonclinical Safety is responsible for designing and implementing overall nonclinical safety strategy to support the development and eventual marketing approval and post-marketing safety for the breadth of the BMS portfolio
Job Summary
Nonclinical Safety is responsible for designing and implementing overall nonclinical safety strategy to support the development and eventual marketing approval and post-marketing safety for the breadth of the BMS portfolio.
The role involves oversight of nonclinical safety evaluation programs, assisting in study design and reporting, and acting as a Nonclinical Safety representative on project development teams.
Bristol Myers Squibb offers a wide variety of competitive benefits, services and programs that provide employees with resources to pursue their goals, both at work and in their personal lives.
Matching Summary
Nonclinical Safety is responsible for designing and implementing overall nonclinical safety strategy to support the development and eventual marketing approval and post-marketing safety for the breadth of the BMS portfolio.
Salary
Brisbane - CA - US: $205,490 - $249,003; Cambridge Crossing: $205,490 - $249,003; New Brunswick - NJ - US: $178,690 - $216,527; Princeton - NJ - US: $178,690 - $216,527; San Diego - CA - US: $196,550 - $238,177; Seattle - WA: $196,550 - $238,177; Not specified
Skills & Requirements
Must-have
Nonclinical safety evaluation programs
Design and reporting of toxicity studies
Regulatory agency interaction
Submission document writing and review
Scientific methodology application
Nice-to-have
Collaborative team environment
Open communication and creativity
Patient-focused innovation
Work-life balance and flexibility
Key Requirements
Bachelor's Degree and 15+ years experience OR Master's Degree and 12+ years experience OR PhD and 8+ years experience
6+ years leadership experience
10+ years regulatory toxicology/development experience
Knowledge of biochemical and mechanistic toxicology
Experience designing and interpreting in vitro and in vivo studies