Executive Director, Toxicology

Added
8 days ago
Type
Full time
Salary
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Related skills

glp regulatory submissions ema fda drug development

πŸ“‹ Description

  • Lead and mentor a team of toxicologists and technical or operational professionals, fostering
  • Define and execute nonclinical safety strategies across discovery, preclinical, IND-enabling, and
  • Provide expert toxicology and safety pharmacology guidance to cross-functional development teams
  • Lead nonclinical sub-teams as an integrated development leader, coordinating activities across
  • Serve as the primary nonclinical representative on Program Development Teams, internal governance
  • Champion program strategy and communicate scientific rationale effectively with senior leadership

🎯 Requirements

  • PhD in Toxicology, Pharmacology, Pathology, DVM, or a related discipline; board certification such
  • 18+ years of experience in pharmaceutical or biotechnology R&D, with a strong track record in
  • Proven ability to operate as an upward-facing nonclinical leader and generalist, with the
  • Deep expertise supporting small-molecule programs across discovery, IND-enabling activities, and
  • Strong working knowledge of national and international GLP guidelines and regulatory expectations.
  • Demonstrated experience defining and executing nonclinical safety strategies across diverse

🎁 Benefits

  • Anticipated annual compensation of $153,000–$290,400, depending on education, experience, skills
  • Eligibility for a company bonus, based in part on organizational and individual performance.
  • 401(k) plan and pension benefits.
  • Vacation benefits and certain time-off and leave benefits.
  • Eligibility for medical, dental, vision, and prescription drug coverage.
  • Flexible benefits, including healthcare and/or dependent day-care flexible spending accounts.
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