Senior Research Scientist
Nonclinical Safety
Confirmed live in the last 24 hours
Locations
Vancouver, BC, Canada
Experience Level
Entry
Junior
Mid
Senior
Expert
Desired Skills
Communications
Requirements
- 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
Company Overview
AbCellera Biologics is a biotechnology company that develops antibody therapeutics to improve patient outcomes.