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Associate Director, Toxicology

Denali Therapeutics
Full-time
Remote friendly (South San Francisco, CA)
United States
$203,000 - $240,000 USD yearly
Clinical Research and Development

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Role Summary

Associate Director, Toxicology responsible for driving nonclinical safety assessment of small and large molecule therapeutics, conducting and managing toxicology studies, analyzing safety data, and collaborating with cross-functional teams to advance drug candidates. Serves as a functional leader for the Toxicology team with people leadership accountability for one or more Toxicologists.

Responsibilities

  • Design and implement nonclinical toxicology programs and strategies to evaluate the safety of therapeutic candidates.
  • Conduct and oversee non-GLP and GLP toxicology studies, ensuring adherence to regulatory standards.
  • Analyze, interpret, and summarize toxicology data to support safety evaluations.
  • Prepare and present safety data to internal project teams and senior management, contributing to informed decision-making.
  • Assist in the preparation and authoring of regulatory documents related to nonclinical safety assessments.
  • Ensure compliance with relevant regulatory guidelines and standards throughout all stages of toxicology studies.
  • Work closely with colleagues in Research and Development, providing toxicology expertise to support cross-functional project teams.
  • Participate in project meetings, offering insights and recommendations to advance safety assessment strategies.
  • Support investigative efforts into mechanisms of toxicity and contribute to the development of safer therapeutic candidates.
  • Assist in developing and implementing de-risking strategies for drug discovery and development projects.
  • Lead direct report(s) through annual goal setting, growth planning, adherence to company policies, and training compliance, providing ongoing feedback on growth and development.

Qualifications

  • PhD or advanced degree in Toxicology, Biology, Pharmacology, or related scientific discipline.
  • Approximately 7+ years of relevant work experience (including postdoctoral work) or MS with 10+ years of relevant experience.
  • Experience with biologics and oligonucleotides preferred.
  • Strong scientific background and scientific aptitude.
  • Excellent critical thinking and scientific skills.
  • Ability to work effectively and collaboratively on cross-functional project teams and a can-do attitude.
  • Ability to work in a fast-paced environment.
  • Excellent oral, presentation, and written communication skills.
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