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Director, Nonclinical Safety

Gilead
Foster City, CA
USD 226,185 - 292,710 / year

About this role

Job title: Director, Nonclinical Safety

About the Role Gilead is seeking a Director to lead the Nonclinical Safety group. The role serves as the toxicology representative on multifunctional project teams, owns the nonclinical safety program, and contributes to regulatory documents to support drug development candidates across multiple platforms from early research through registration and post-approval. The position leads non-clinical development sub-teams and collaborates to integrate early nonclinical safety strategies throughout Research. A fast-paced, data-driven environment requires scientific rigor, strategic thinking, and strong cross-functional collaboration.

What You'll Do

  • Serve as the toxicology representative on multifunctional project teams and own the nonclinical safety program
  • Contribute to regulatory documents to support global regulatory filings
  • Manage multiple projects with minimal supervision and oversee protocol/data/study reports
  • Interpret data in the context of literature and project goals; provide independent technical contributions
  • Lead Non-Clinical Development sub-teams and participate in process improvement initiatives
  • Communicate effectively cross-functionally to achieve company goals; act as a team player in a high-speed environment
  • Support integration of early nonclinical safety strategies throughout Research

What We're Looking For

  • PhD in a related scientific discipline with 12+ years of experience in nonclinical safety/toxicology
  • Experience with NAMs and AI pertaining to nonclinical toxicology (highly desirable)
  • BS or MS degree with extensive industry experience
  • Experience writing and reviewing regulatory documents to support global regulatory filings
  • Ability to manage multiple projects with minimal supervision; strong data interpretation skills
  • Excellent cross-functional communication and leadership capabilities

Nice to Have

  • Leadership of cross-functional teams and ability to drive process improvements
  • Experience in regulatory submissions and interaction with regulatory agencies

Compensation & Benefits

  • Salary range: $226,185 - $292,710 per year (USD)
  • Eligible for discretionary annual bonus and discretionary stock-based long-term incentives (eligibility varies by role)
  • Paid time off and a benefits package including company-sponsored medical, dental, vision, and life insurance plans
  • For more benefits information, see the company website

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