Director, Nonclinical Safety

Gilead Sciences

California, United States
Base: $226,185.00 - $292,710.00; bonus/equity: dis...
On-site
Toxicology representative on project teams
Nonclinical safety program ownership
Regulatory document contribution
Gilead Sciences is seeking a Director of Nonclinical Safety to lead their nonclinical safety programs and contribute to regulatory documents that support drug development. The ideal candidate will have over 12 years of experience in a relevant scientific discipline, with a strong emphasis on collaboration, problem-solving, and strategic oversight within a fast-paced environment

Job Summary

  • The primary responsibility is to serve as the toxicology representative on multifunctional project teams, including ownership of the nonclinical safety program and contributing to regulatory documents to support drug development candidates across a variety of platforms from early research through registration/post approval.
  • Plays key role on cross functional teams – both Research and Development Project Teams where he/she is responsible for design, implementation, oversight and analysis of nonclinical programs to support drug development candidates across a variety of platforms.
  • Gilead is a fast-paced, data-driven, scientifically rigorous organization, and the role will suit a scientist who is able to thrive in this type of environment.

Matching Summary

Match Score: 85

Gilead Sciences is seeking a Director of Nonclinical Safety to lead their nonclinical safety programs and contribute to regulatory documents that support drug development. The ideal candidate will have over 12 years of experience in a relevant scientific discipline, with a strong emphasis on collaboration, problem-solving, and strategic oversight within a fast-paced environment.

Salary

Base: $226,185.00 - $292,710.00; Bonus/Equity: discretionary annual bonus, discretionary stock-based long-term incentives; Benefits: company-sponsored medical, dental, vision, and life insurance plans

Skills & Requirements

Must-have

  • toxicology representative on project teams
  • nonclinical safety program ownership
  • regulatory document contribution
  • cross-functional team leadership
  • complex problem solving
  • process improvement initiatives

Nice-to-have

  • thrive in fast-paced environment
  • nurture a culture of innovation
  • independent technical contributions

Key Requirements

  • 12+ years of experience with PhD
  • Experience with NAM's and AI highly desirable
  • BS or MS degree with extensive industry experience

Work Rights

Not specified

Tailored Resume

Cover Letter