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- Tasks: Lead genetic toxicology studies and collaborate on drug safety assessments.
- Company: Join Novartis, a global leader in innovative pharmaceutical research.
- Benefits: Enjoy competitive rewards, diverse teams, and a commitment to inclusion.
- Why this job: Make a real impact on drug safety and patient lives while working with cutting-edge technology.
- Qualifications: PhD or DVM required, with 5+ years in regulatory genetic toxicology.
- Other info: Position available in the US or UK; remote work options may be considered.
The predicted salary is between 43200 - 72000 £ per year.
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. More than 100,000 people across 140 countries are working for Novartis to discover, develop, and successfully market innovative products to prevent and cure diseases, ease suffering, and enhance the quality of life.
As a Genetic Toxicology expert at Novartis, you will play a key role in supporting non-clinical safety assessment throughout drug discovery and development, as well as for established medicines, with state-of-the-art regulatory compliance. Utilizing your expertise, you will collaborate with cross-functional teams to ensure the delivery of high-quality and compliant research. The position can be located in the US (Cambridge, MA or East Hanover, NJ) or UK (London).
Key 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.
Essential 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.
Desirable Requirements:
- Strong data exploration and analysis skills.
Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve.
Associate Director - Genetic Toxicology Expert employer: Novartis
Contact Detail:
Novartis Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Associate Director - Genetic Toxicology Expert
✨Tip Number 1
Network with professionals in the genetic toxicology field. Attend relevant conferences, webinars, or workshops where you can meet experts and learn about the latest trends and technologies. This will not only enhance your knowledge but also help you make valuable connections that could lead to job opportunities.
✨Tip Number 2
Stay updated on regulatory guidelines and advancements in genetic toxicology. Follow industry publications, join professional associations, and participate in online forums. Demonstrating your knowledge of current regulations during interviews can set you apart from other candidates.
✨Tip Number 3
Prepare to discuss your experience with cross-functional teams. Highlight specific projects where you collaborated with different departments, showcasing your ability to communicate effectively and lead initiatives. This is crucial for a role that requires teamwork and collaboration.
✨Tip Number 4
Research Novartis' recent projects and initiatives in drug safety and genetic toxicology. Understanding their current focus areas will allow you to tailor your discussions during interviews, demonstrating your genuine interest in the company and how your expertise aligns with their goals.
We think you need these skills to ace Associate Director - Genetic Toxicology Expert
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights your experience in genetic toxicology and drug development. Emphasise any relevant projects or roles that demonstrate your expertise and analytical skills.
Craft a Compelling Cover Letter: Write a cover letter that showcases your passion for pharmaceutical research and drug safety. Mention specific experiences that align with the responsibilities outlined in the job description, such as leading cross-functional teams or engaging with regulatory bodies.
Highlight Relevant Skills: In your application, clearly outline your skills related to genetic toxicology, data analysis, and communication. Use examples from your past work to illustrate how these skills have contributed to successful outcomes in your projects.
Showcase Continuous Learning: Mention any recent training, certifications, or workshops you have attended that relate to genetic toxicology or regulatory compliance. This demonstrates your commitment to staying updated in the field and your dedication to scientific excellence.
How to prepare for a job interview at Novartis
✨Showcase Your Expertise
Make sure to highlight your extensive knowledge in genetic toxicology. Be prepared to discuss specific studies you've conducted and how they relate to drug discovery and development, as this will demonstrate your capability to contribute effectively to the team.
✨Understand Regulatory Compliance
Familiarise yourself with the relevant regulatory guidelines and standards in genetic toxicology. Being able to articulate your understanding of these regulations during the interview will show that you are well-prepared for the role and can ensure compliance in your work.
✨Emphasise Collaboration Skills
Since the role involves leading cross-functional teams, be ready to provide examples of how you've successfully collaborated with others in past projects. Highlight your communication skills and how you engage with both internal and external partners.
✨Prepare for Technical Questions
Expect to face technical questions related to genetic toxicity assessments and data interpretation. Brush up on your analytical skills and be ready to discuss how you approach problem-solving in complex scenarios, as this will reflect your commitment to scientific excellence.
