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- Tasks: Lead and monitor toxicology studies while gaining expertise in regulatory toxicology.
- Company: Join a forward-thinking team focused on innovation and development.
- Benefits: Competitive salary, home-based work, and comprehensive regulatory training.
- Why this job: Make a real impact in safety assessments and advance your career in toxicology.
- Qualifications: Experience in GLP toxicology studies and a passion for non-animal methods.
- Other info: Exciting opportunity for career growth in a dynamic scientific environment.
The predicted salary is between 36000 - 60000 £ per year.
Location: UK home base, Home Based
Competitive salary + regulatory training
Description: An opportunity for a Toxicology Study Director or Scientist to move to a desk based Regulatory Toxicology role. You will use your expert knowledge of GLP study protocols to place and monitor studies with partner CROs – you will gain full training in the safety and risk assessment aspects of the role.
You will join an in-house team of toxicology and ecotoxicology specialists providing expert support to internal departments. They place a lot of studies to generate new data and would like to recruit a study protocol expert who can help in the placement and monitoring of studies. The vast majority of placed studies are in-vitro or in-silico – specific experience of a range of NAMs, in-vitro and in-silico methods would be highly attractive.
The team believes in development and innovation – you will receive full training in the safety and risk assessment aspects – and be encouraged to keep up to date with new emerging non-animal methods.
We are looking for a Study Director or Study Scientist with a proven track record in managing GLP toxicology studies – ideally you will have experience with a range of in-vitro protocols and be interested in furthering your expertise in this area. An excellent career development opportunity.
Key Skills:
- Toxicology
- Safety assessment
- Hazard assessment
- Regulatory toxicology
- NAM
- In-vitro
- In-silico methods
- Innovation
- Toxicology support
- Presentation
- Regulatory science
- Method innovation
- Communication
Toxicology Study Director – move into Regulatory Toxicology in London employer: VRS Recruitment
Contact Detail:
VRS Recruitment Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Toxicology Study Director – move into Regulatory Toxicology in London
✨Tip Number 1
Network like a pro! Reach out to professionals in the regulatory toxicology field on LinkedIn or at industry events. We can’t stress enough how valuable personal connections can be in landing that dream job.
✨Tip Number 2
Prepare for interviews by brushing up on your knowledge of GLP study protocols and in-vitro methods. We recommend practising common interview questions with a friend or even in front of the mirror to boost your confidence.
✨Tip Number 3
Showcase your passion for innovation in toxicology during interviews. We want to see how you stay updated with emerging non-animal methods and how you can contribute to our team's development goals.
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets noticed. Plus, we love seeing candidates who take the initiative to connect directly with us.
We think you need these skills to ace Toxicology Study Director – move into Regulatory Toxicology in London
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights your experience with GLP study protocols and any relevant in-vitro or in-silico methods. We want to see how your background aligns with the role, so don’t be shy about showcasing your expertise!
Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you’re excited about moving into Regulatory Toxicology and how your skills can contribute to our team. Keep it engaging and personal – we love to see your passion!
Showcase Your Communication Skills: Since this role involves working with various teams, highlight your communication skills in your application. Whether it’s through your CV or cover letter, let us know how you’ve effectively collaborated in the past.
Apply Through Our Website: We encourage you to apply directly through our website for a smoother process. It helps us keep track of your application and ensures you don’t miss out on any important updates from us!
How to prepare for a job interview at VRS Recruitment
✨Know Your GLP Protocols
Make sure you brush up on your knowledge of Good Laboratory Practice (GLP) study protocols. Be ready to discuss how you've applied these in your previous roles, especially in managing toxicology studies. This will show that you’re not just familiar with the concepts but can also implement them effectively.
✨Familiarise Yourself with NAMs
Since the role involves in-vitro and in-silico methods, it’s crucial to have a solid understanding of New Approach Methodologies (NAMs). Prepare examples of how you’ve used these methods in past projects, and be ready to discuss their advantages and limitations during the interview.
✨Show Your Passion for Innovation
The team values development and innovation, so come prepared to share your thoughts on emerging non-animal methods in toxicology. Discuss any recent advancements you’ve followed and how they could impact regulatory toxicology. This will demonstrate your enthusiasm for the field and your commitment to staying current.
✨Practice Your Communication Skills
As a Study Director, you'll need to communicate complex information clearly. Practice explaining your past projects or findings in simple terms, as if you were presenting to someone outside your field. This will help you convey your expertise effectively and show that you can support internal departments with clarity.
