Support non-clinical safety assessment throughout drug discovery and development, as well as for established medicines, with state-of-the-art regulatory compliance
Job Summary
Support non-clinical safety assessment throughout drug discovery and development, as well as for established medicines, with state-of-the-art regulatory compliance.
Develop and implement state-of-the-art innovative technologies and systems for regulatory and investigative genetic toxicity testing across all therapeutic areas and modalities.
US-based eligible employees will receive a comprehensive benefits package that includes health, life and disability benefits, a 401(k) with company contribution and match, and a variety of other benefits.
Matching Summary
Support non-clinical safety assessment throughout drug discovery and development, as well as for established medicines, with state-of-the-art regulatory compliance.
Salary
Base: $185,500 - $344,500; Bonus/Equity: performance-based cash incentive and eligibility for annual equity awards; Benefits: comprehensive benefits package including health, life and disability benefits, a 401(k) with company contribution and match, generous time off package
Skills & Requirements
Must-have
genetic toxicology studies
drug discovery and development
regulatory compliance
cross-functional teams
health authority interactions
Nice-to-have
advancing pharmaceutical research
ensuring drug safety
state-of-the-art technologies
scientific excellence
bold innovation through collaboration
Key Requirements
PhD, DVM or equivalent
Minimum of 15 years of demonstrated experience
Work experience in pharmaceutical companies or CRO Laboratories