Director of Genetic Toxicology & Regulatory Strategy

Novartis AG; City of Westminster; On-site; GBP 70,000 - 100,000; Full time

Job summary

A leading pharmaceutical company is seeking an experienced Genetic Toxicologist to advance pharmaceutical research and ensure drug safety. Candidates should have a PhD or DVM, with strong expertise in genetic toxicology and a minimum of 15 years of experience. You will conduct genetic toxicology studies, provide expert opinions for regulatory submissions, and lead cross-functional teams. This position offers an opportunity to engage with various stakeholders and stay at the forefront of emerging technologies in the field.

Qualifications

• 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 preferred.
• Experience in pharmaceutical companies or CRO Laboratories servicing pharmaceuticals.
• Extensive experience in health authority interactions.
• Strong data exploration and analytical skills.
• Exceptional analytical, communication, and collaboration skills.

Responsibilities

• Conduct and monitor genetic toxicology studies and interpret data.
• Provide expert opinions on genetic toxicity assessments.
• Develop and implement innovative technologies for genetic toxicity testing.
• Maintain scientific and regulatory expertise in Genetic Toxicology.
• Lead cross-functional teams and represent the PCS line function.
• Engage and collaborate with key internal and external partners.
• Ensure compliance with relevant regulatory guidelines.
• Stay updated on emerging technologies in genetic toxicology.

Job description

A leading pharmaceutical company is seeking an experienced Genetic Toxicologist to advance pharmaceutical research and ensure drug safety. Candidates should have a PhD or DVM, with strong expertise in genetic toxicology and a minimum of 15 years of experience. You will conduct genetic toxicology studies, provide expert opinions for regulatory submissions, and lead cross-functional teams. This position offers an opportunity to engage with various stakeholders and stay at the forefront of emerging technologies in the field.