Director, Nonclinical Safety Assessment Expert (multiple Therapeutic Areas)

Novartis

Cambridge, MA, US
Base: $185,500 - $344,500 py; bonus/equity: perfor...
Hybrid
Nonclinical safety leadership
Global health authority interaction
Multiple therapeutic area expertise
Novartis is seeking a Director of Nonclinical Safety Assessment to provide leadership in safety strategies across various therapeutic areas, ensuring compliance and facilitating successful clinical trial initiation. The role requires extensive experience in nonclinical drug development and direct interaction with global health authorities

Job Summary

  • This role provides global, end-to-end nonclinical safety leadership ensuring scientifically robust strategies for successful clinical trial initiation and registration.
  • The incumbent will serve as the primary Preclinical Safety authority on cross-functional R&D teams and lead interactions with global Health Authorities.
  • Compensation includes a performance-based cash incentive, potential annual equity awards, and a comprehensive benefits package including health and 401(k) matching.

Matching Summary

Match Score: 85

Novartis is seeking a Director of Nonclinical Safety Assessment to provide leadership in safety strategies across various therapeutic areas, ensuring compliance and facilitating successful clinical trial initiation. The role requires extensive experience in nonclinical drug development and direct interaction with global health authorities.

Salary

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

Skills & Requirements

Must-have

  • Nonclinical safety leadership
  • Global Health Authority interaction
  • Multiple therapeutic area expertise
  • Small molecules and biotherapeutics
  • IND/NDA submission writing

Nice-to-have

  • Cross-functional R&D collaboration
  • In-licensing opportunity evaluation
  • Mentorship and coaching skills
  • Strategic integration capabilities

Key Requirements

  • Advanced scientific degree (PhD, MD, DVM, PharmD)
  • 8+ years experience in nonclinical drug development
  • 5+ years as nonclinical safety Project Team member
  • Proven track record with global Health Authorities
  • Expertise across small molecules and biotherapeutics

Work Rights

Not specified

Tailored Resume

Cover Letter