Genetic Toxicologist at Novartis ensuring drug safety by supporting non-clinical safety assessment throughout drug discovery and development. Collaborating with cross-functional teams to deliver compliant research.
Responsibilities
Conduct and monitor genetic toxicology studies and interpret data to support drug discovery and development programs spanning all therapeutic modalities and disease indications
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
Engaging and collaborating with key internal and external customer partners
Ensure compliance with relevant regulatory guidelines and standards
Stay at the forefront of emerging technologies in genetic toxicology
Requirements
PhD, DVM or equivalent
Strong knowledge in genetic toxicology
Excellent knowledge of the drug development process
Minimum of 15 years of demonstrated experience in regulatory and investigative genetic toxicology is strongly preferred
Work experience in pharmaceutical companies or CRO Laboratories servicing pharmaceuticals
Extensive experience in health authority interactions
Strong data exploration, analytical skills and commitment to scientific excellence
Exceptional analytical, communication and collaboration skills
Benefits
health insurance
life and disability benefits
401(k) with company contribution and match
generous time off package including vacation, personal days, holidays and other leaves
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