Senior Research Scientist - Toxicology

Each of us cares about someone who will need medicines. That’s why our vision is to repeatedly beat the odds to deliver breakthrough medicines to patients that need them. We pursue truth and scientific rigour and have the courage to work at the edge of the unknown.

• 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 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

• 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 is highly desirable, but not required.

AbCellera’s hiring range for this role is CAD $115,000 – $143,000 annually, commensurate with education and job‑related knowledge, skills, and experience. In addition to base salary, the package includes equity, an annual bonus dependent on team and company performance, and a 6% non‑match RRSP contribution.

The role also provides a CAD $1,500 annual Active Lifestyle Allowance, annual vacation, professional development opportunities, and comprehensive health benefits. Scientific and technical mentorship is a priority, and employees experience a strong sense of community and connections through work, clubs, and social events.

AbCellera is a clinical‑stage biotechnology company focused on discovering and developing antibody‑based medicines in the areas of endocrinology, women’s health, immunology, and oncology. The company prepares to advance antibody drug programs from target to clinic through its platform and internal pipeline, which includes two drug candidates in clinical development, two preclinical development candidates (DCs) in IND‑enabling activities, and more than 20 discovery programs across multiple modalities and indications.