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Research Scientist II - Toxicology

External
abcellera logoAbcellera · Vancouver, Canada
$100K–$125K/yrFull-timeOn-site1w ago
CADDocumentation
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Benefits

About AbCelleraCreating medicines is the most important work we can do.Today, our pipeline includes two drug candidates in clinical development, two preclinical development candidates (DCs) in Investigational New Drug (IND)-enabling activities, and more than 20 active discovery programs across multiple modalities and indications.We believe that when tenacious people share a vision and work together, they can truly have a positive impact. That's why we hire for character and intelligence, not just for CVs or experience.We look for people with drive and energy. People we trust. People who need to know their days are being well spent. That their work really matters. In the end, our success will be measured by the impact of our medicines.To applyHealth insuranceVision insurancePaid time offEquity / stock optionsPerformance bonus

Additional Information

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. We are looking for a dynamic and detail-oriented Research Scientist II 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. How you might spend your days Designing, planning, and supporting the execution of in vitro and/or in vivo toxicology studies as needed, adhering to the appropriate regulatory guidelines and communicating toxicology study results internally Updating and maintaining proper recording of nonclinical safety study data, as required by Good Laboratory Practice (GLP) Assisting with the authoring of toxicology sections of Regulatory documentation Collaborating with scientists across various teams at AbCellera to ensure high data quality and that studies meet the company's objectives Contributing to the development of our toxicology programs and participating as a nonclinical safety/toxicology representative as needed Maintaining an active scan of published toxicology data relevant to AbCellera's product portfolio, and continuously expanding your knowledge base We'd love to hear from you if You hold a PhD in Toxicology or related biological science field, and have a minimum of 2-5 years of related experience in an academic or industry environment; candidates with a MSc and 7+ years of relevant experience will also be considered You have hands-on experience with in vitro and/or in vivo toxicology studies You have a strong desire to learn and develop proficiency with nonclinical safety assessment of large molecules/biologics You have strong analytical and problem-solving skills You have excellent communication and collaboration skills


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