Facebook pixel

Senior Research Scientist
Nonclinical Safety
Confirmed live in the last 24 hours
Vancouver, BC, Canada
Experience Level
Desired Skills
  • Performing nonclinical safety assessment activities throughout all stages of antibody drug development
  • Monitoring nonclinical studies, interpreting data, generating reports and contributing to the generation of regulatory reports
  • Preparing nonclinical safety sections and strategy that support IND and clinical trial applications
  • Collaborating with teams across the company to solve problems, analyze, interpret and communicate data
  • Evaluating new technology and testing new models to better predict human illness
  • Reporting findings to our teams and partners to support data-driven decision making
  • You are genuinely curious, with an interest in discussing innovative ideas in a highly collaborative and face paced environment
  • You are good at communicating scientific and/or technical concepts with an emphasis on application
  • You are strongly self-motivated and work independently to identify project needs and follow that up with constructing and implementing solutions
  • You enjoy the teamwork that comes with working on complicated biological questions and building data sets that help to predict the success of therapies
  • PhD in Toxicology or related discipline with working knowledge of the drug development process with 8+ years practical work experience in a biopharmaceutical industry environment
  • Ability to perform scientific investigation of fundamental toxicology issues, either through review of the academic literature or empirical drug development experience
  • Demonstrated proficiency in nonclinical safety assessment of large molecules/biologics from discovery to mid-stage development
  • Significant experience with authoring/reviewing study protocols and reports to ensure appropriate toxicology datasets are accurately generated and interpreted
  • Exceptional analytical and problem-solving capabilities
  • Understanding of regulatory processes, GLP/ICH and other regulatory guidance documents, and basic knowledge of regulatory toxicology
  • Excellent documentation, organizational and communication skills
  • Proven interpersonal skills with the ability to work collaboratively as a member of a cross-functional team
Desired Qualifications
  • Experience with assessing new and emerging in silico / in vitro technologies to improve human safety prediction for the therapeutic antibody development process
  • Experience generating impurity safety risk assessments
  • Exceptional writing skills
  • Experience with early-stage R&D of immuno-oncology therapeutics
AbCellera Biologics
Company Overview
AbCellera Biologics is a biotechnology company that develops antibody therapeutics to improve patient outcomes.