Director, Nonclinical Safety Assessment Expert (multiple Therapeutic Areas)

Novartis

Cambridge, MA, United States
Base: $185,500 - $344,500 py; bonus/equity: perfor...
Hybrid
Nonclinical safety assessment programs
Global health authority interactions
Cross functional r&d collaboration
In this key role you will provide global, end to end nonclinical safety leadership across multiple therapeutic areas and modalities, ensuring scientifically robust, fit for purpose, and regulatory compliant safety strategies that enable successful clinical trial initiation and support registration

Job Summary

  • In this key role you will provide global, end to end nonclinical safety leadership across multiple therapeutic areas and modalities, ensuring scientifically robust, fit for purpose, and regulatory compliant safety strategies that enable successful clinical trial initiation and support registration.
  • You will serve as the primary Preclinical Safety authority on cross functional R&D teams and in interactions with global Health Authorities, enabling portfolio progression and strategic integration across therapeutic areas.
  • US-based eligible employees will receive a comprehensive benefits package that includes health, life and disability benefits, a 401(k) with company contribution and match, and a variety of other benefits along with a generous time off package.

Matching Summary

In this key role you will provide global, end to end nonclinical safety leadership across multiple therapeutic areas and modalities, ensuring scientifically robust, fit for purpose, and regulatory compliant safety strategies that enable successful clinical trial initiation and support registration.

Salary

Base: $185,500 - $344,500 per year; Bonus/Equity: Performance-based cash incentive and eligibility for annual equity awards; Benefits: Comprehensive health, life, disability benefits, 401(k) with company match, generous time off

Skills & Requirements

Must-have

  • Nonclinical safety assessment programs
  • Global Health Authority interactions
  • Cross functional R&D collaboration
  • Regulatory compliant safety strategies
  • Leadership in matrix managed environments
  • Safety strategy for multiple modalities

Nice-to-have

  • Mentorship and coaching
  • Drug development strategy
  • Communication strategy coordination
  • In licensing and out licensing support
  • Participation in cross functional initiatives

Key Requirements

  • Advanced scientific degree or equivalent industry experience
  • 5+ years nonclinical safety Project Team experience
  • 8+ years nonclinical drug development experience
  • Expertise across multiple modalities
  • Proven global Health Authority interaction experience
  • Demonstrated leadership in international projects

Work Rights

Not specified

Tailored Resume

Cover Letter