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AbCelleraNew
Overview
The role involves designing and executing in vitro and in vivo toxicology studies to assess the safety of drug candidates. Responsibilities include maintaining GLP-compliant data and authoring toxicology sections for regulatory documentation.
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Compensation
CA$100,000 - CA$125,000 / YEAR
Posted
New
Lead the design and oversight of in vitro and in vivo toxicology studies to assess the safety of drug candidates. Serve as a subject matter expert for nonclinical safety, authoring regulatory documentation and providing risk-benefit evaluations to leadership.
CA$112,000 - CA$150,000 / YEAR
