Salary
💰 $152,600 - $283,400 per year
About the role
- Conduct and monitor genetic toxicology studies and interpret data to support drug discovery and development programs
- Provide expert opinions on genetic toxicity assessments to support drug discovery and development project teams, regulatory submissions and due diligences, and life-cycle management of established medicines
- Develop and implement state-of-the-art innovative technologies and systems for regulatory and investigative genetic toxicity testing across all therapeutic areas and modalities
- Maintain state-of-the-art scientific and regulatory expertise in Genetic Toxicology
- Lead cross-functional teams; represent the PCS line function on internal and external boards; actively share and communicate information back to the Genetic Toxicology team
- Engage and collaborate with key internal and external customer partners
- Ensure compliance with relevant regulatory guidelines and standards
Requirements
- PhD, DVM or equivalent
- Broad knowledge in genetic toxicology
- Knowledge of the drug development process
- Minimum of 5 years of experience in regulatory genetic toxicology
- Experience in health authority interactions
- Strong analytical skills and a commitment to scientific excellence
- Excellent communication and team collaboration skills