Director/associate Director, Toxicology

Calicolabs

South San Francisco, CA, United States
Base: $235,000 - $315,000; bonus: two annual cash ...
On-site (at least 4 days a week)
Nonclinical safety leadership experience
Design and oversight of glp toxicity studies
Authoring global regulatory submission documents
Calico Labs is seeking a Director/Associate Director of Toxicology to lead nonclinical safety efforts in their innovative research environment focused on human aging. The ideal candidate will possess significant experience in regulatory toxicology and successfully contribute to preclinical development projects

Job Summary

  • Calico is an Alphabet-founded research company dedicated to harnessing advanced technologies to understand human aging and develop interventions for longer, healthier lives.
  • The Nonclinical Safety Leader will act as a subject matter expert representing toxicology on project teams to support early- and late-stage drug development.
  • This role requires overseeing the design and reporting of toxicity studies while ensuring compliance with Good Laboratory Practice and FDA/ICH guidelines.

Matching Summary

Match Score: 85

Calico Labs is seeking a Director/Associate Director of Toxicology to lead nonclinical safety efforts in their innovative research environment focused on human aging. The ideal candidate will possess significant experience in regulatory toxicology and successfully contribute to preclinical development projects.

Salary

Base: $235,000 - $315,000; Bonus: Two annual cash bonuses eligible; Benefits: Not specified

Skills & Requirements

Must-have

  • Nonclinical safety leadership experience
  • Design and oversight of GLP toxicity studies
  • Authoring global regulatory submission documents
  • Risk assessment of target pharmacology toxicity
  • Collaboration with multi-disciplinary project teams

Nice-to-have

  • Experience with advanced in vitro models
  • Knowledge of new approach methodologies (NAMs)
  • Self-motivated and highly adaptable mindset
  • Ability to pivot strategies in fast-paced environment

Key Requirements

  • PhD in Toxicology or related discipline
  • 8+ years of regulatory toxicology experience
  • Board certification (e.g., DABT)
  • Track record of progressing candidates to clinical development
  • Extensive knowledge of GLP principles and FDA/ICH guidelines

Work Rights

Not specified

Tailored Resume

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