CSL Ltd is seeking a Principal Scientist in Regulatory Toxicology to lead nonclinical safety strategies for drug development projects. The ideal candidate will have extensive experience in toxicology, regulatory submissions, and cross-functional collaboration in the pharmaceutical or biotech industry
Job Summary
The Principal Toxicologist will lead nonclinical safety strategies across multiple drug development projects from early discovery through regulatory submission.
This role serves as the primary representative on interdisciplinary teams and leads the Nonclinical Expert Team to ensure scientific leadership.
CSL is building a future-ready team that thrives in dynamic biotech ecosystems committed to developing therapies that make a meaningful difference worldwide.
Matching Summary
Match Score: 85
CSL Ltd is seeking a Principal Scientist in Regulatory Toxicology to lead nonclinical safety strategies for drug development projects. The ideal candidate will have extensive experience in toxicology, regulatory submissions, and cross-functional collaboration in the pharmaceutical or biotech industry.
Skills & Requirements
Must-have
Nonclinical safety assessment
Regulatory submission documents
GLP and non-GLP study oversight
Cross-functional team leadership
ICH and FDA guideline knowledge
Nice-to-have
Board Certification ERT or DABT
Experience with CSL therapeutic areas
Multiple therapeutic modalities experience
Agile team collaboration skills
Key Requirements
PhD, DVM, or equivalent in Toxicology
5-8 years pharmaceutical or biotech industry experience