Director - Genetic Toxicology Expert

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

Are you passionate about advancing pharmaceutical research and ensuring drug safety at Novartis? The Preclinical Safety (PCS) department at Novartis BioMedical Research (BR) is seeking an experienced Genetic Toxicologist to join our dynamic team.

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.
• Engage and collaborate 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.

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 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.

Learn more about Novartis: https://www.novartis.com/about/strategy/people-and-culture. Benefits and rewards information: https://www.novartis.com/careers/benefits-rewards. Diversity and Inclusion: Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve.