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Senior Research Scientist - Toxicology

Canada, Vancouver 112000.00 - 150000.00 CAD / Year · Job Posted June 15, 2026
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Job Description

We are looking for a dynamic and detail-oriented Senior Research Scientist to join our growing Nonclinical Safety team. You will be responsible for supporting our team's efforts in developing and executing toxicology studies to assess the safety of our drug candidates. For this role, you will require a strong understanding of toxicology principles as well as hands-on experience with in vitro and/or in vivo studies.

Job Responsibility

  • Leading the design, planning, and oversight of in vitro safety and/or in vivo toxicology studies, ensuring alignment with global regulatory guidelines and strategic company objectives
  • Serving as a subject matter expert (SME) for Nonclinical Safety within cross-functional project teams, actively representing the function in internal and external stakeholder meetings
  • Providing critical assessment of complex toxicology data, translating and communicating clear, actionable risk-benefit evaluations and strategic recommendations to project teams and executive leadership
  • Maintaining comprehensive and meticulous recording of nonclinical safety study data as required by Good Laboratory Practice (GLP)
  • Authoring and critically reviewing the in vitro safety, toxicology, and safety pharmacology sections of Regulatory documentation (such as INDs, CTAs, IBs, and BLAs)
  • Collaborating seamlessly with scientists across various matrixed teams at AbCellera to ensure high data quality and accelerate program advancement
  • Contributing to the development of our toxicology programs and performing as a nonclinical safety/toxicology representative as needed
  • Maintaining an active scan and synthesis of published toxicology literature and evolving regulatory guidance relevant to AbCellera’s product portfolio, translating insights into internal best practices

Requirements

  • PhD in Toxicology or a related field, and a minimum of 5-8 years of related industry experience supporting biologics development
  • candidates with a MSc and 10+ years of relevant experience will also be considered
  • extensive hands-on experience with in vitro and/or in vivo toxicology studies
  • demonstrated proficiency with nonclinical safety assessment of large molecules/ biologics
  • strong organizational, critical problem-solving, and analytical skills to assess complex datasets and propose strategic solutions
  • excellent scientific writing, communication, and collaboration skills to effectively lead scientific discussions and influence decision-making
  • DABT accreditation (highly desirable, but not required)

Nice to have

DABT accreditation

What we offer

  • Equity
  • annual bonus dependent on team and company performance
  • 6% (non-match) RRSP contribution
  • CAD $1,500 annual Active Lifestyle Allowance
  • annual vacation
  • professional development opportunities
  • comprehensive health benefits
  • Scientific and technical mentorship
  • strong sense of community and connections through work, clubs, and socials

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