At a Glance
- Tasks: Lead nonclinical safety strategy and oversee toxicology studies in a fast-paced biotech environment.
- Company: Dynamic recruitment agency connecting top talent with innovative biotech firms.
- Benefits: High-impact role with significant scientific ownership and influence on development strategy.
- Other info: Ideal for those seeking broader visibility and influence in an ambitious biotech.
- Why this job: Shape and scale nonclinical safety capabilities in a high-potential clinical pipeline.
- Qualifications: Significant toxicology experience and strong small molecule development expertise required.
The predicted salary is between 80000 - 100000 £ per year.
REMOTE - UK - Director, Toxicologist
Northreach is a dynamic recruitment agency that connects businesses with top talent in the Life Science sectors. We specialize in providing a seamless recruitment experience for clients and candidates, fostering innovation and professional growth.
A well-funded, clinical-stage biotech developing innovative small molecule therapies is seeking an experienced Associate Director / Director of Toxicology to lead nonclinical safety strategy across a growing pipeline. We’re looking for a senior toxicology leader who combines strong scientific judgement with hands-on operational execution and thrives in a fast-paced biotech environment.
The Role
You’ll provide strategic and scientific leadership across nonclinical safety activities spanning discovery through clinical development. Key responsibilities include:
- Leading toxicology strategy across candidate selection, IND-enabling studies and clinical-stage development
- Designing, overseeing and interpreting GLP / non-GLP toxicology studies through external CRO partners
- Reviewing protocols, data packages and final reports to ensure scientific rigour and regulatory readiness
- Driving investigative toxicology activities to assess mechanisms and de-risk programmes
- Supporting regulatory submissions and health authority interactions
- Partnering cross-functionally with DMPK, Regulatory, Clinical Development, CMC and Discovery teams
- Presenting toxicology recommendations to senior internal stakeholders
What We’re Looking For
- Significant toxicology experience within biotech, pharma or CRO settings
- Strong small molecule development expertise
- Deep knowledge of IND-enabling toxicology requirements
- Proven CRO oversight and outsourced study management experience
- Ability to critically interpret data and translate findings into clear strategic recommendations
- Comfortable operating with autonomy in a lean, evolving organisation
Highly Desirable
- Investigative / mechanistic toxicology expertise
- Regulatory interaction experience (FDA / MHRA / EMA)
- DABT or equivalent credentials
Why This Opportunity?
This is a genuinely high-impact role offering:
- Significant scientific ownership
- Direct influence on development strategy
- Exposure across a high-potential clinical pipeline
- The chance to help shape and scale nonclinical safety capabilities
- Ideal for someone currently operating at Associate Director / Director level and looking for broader visibility, ownership, and influence within an ambitious biotech.
If this sounds relevant — or you know someone who may be a fit — feel free to get in touch confidentially.
Senior Toxicologist in London employer: Northreach
Contact Detail:
Northreach Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Senior Toxicologist in London
✨Tip Number 1
Network like a pro! Reach out to your connections in the biotech field, attend industry events, and engage with professionals on LinkedIn. We can’t stress enough how important it is to make those personal connections that could lead to job opportunities.
✨Tip Number 2
Prepare for interviews by brushing up on your toxicology knowledge and being ready to discuss your past experiences. We recommend practising common interview questions and having a few examples of your work ready to showcase your expertise.
✨Tip Number 3
Don’t just apply and wait! Follow up on your applications after a week or so. A quick email can show your enthusiasm and keep you on their radar. We believe persistence pays off!
✨Tip Number 4
Check out our website for the latest job openings in the biotech sector. We’re always updating our listings, and applying through us can give you an edge. Let’s land that dream job together!
We think you need these skills to ace Senior Toxicologist in London
Some tips for your application 🫡
Tailor Your CV: Make sure your CV is tailored to highlight your toxicology experience and leadership skills. We want to see how your background aligns with the role, so don’t be shy about showcasing your achievements in biotech or pharma.
Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you’re the perfect fit for this senior role. Share specific examples of your strategic leadership in toxicology and how you've driven success in previous positions.
Showcase Your Scientific Judgement: In your application, emphasise your strong scientific judgement and operational execution. We’re looking for someone who can navigate the complexities of nonclinical safety, so make sure to highlight relevant experiences that demonstrate your expertise.
Apply Through Our Website: We encourage you to apply through our website for a seamless application process. It’s the best way for us to receive your application and ensure it gets the attention it deserves!
How to prepare for a job interview at Northreach
✨Know Your Stuff
Make sure you brush up on your toxicology knowledge, especially around small molecule development and IND-enabling studies. Be ready to discuss specific examples from your past experiences that showcase your scientific judgement and operational execution.
✨Showcase Your Leadership Skills
As a senior toxicologist, you'll need to demonstrate your ability to lead and influence. Prepare to share instances where you've successfully driven toxicology strategy or collaborated with cross-functional teams. Highlight how your leadership has impacted project outcomes.
✨Be Ready for Technical Questions
Expect in-depth questions about GLP/non-GLP studies and regulatory interactions. Familiarise yourself with the latest guidelines from agencies like the FDA and EMA. Being able to interpret data and translate findings into strategic recommendations will be key.
✨Prepare for Cultural Fit
This role is in a fast-paced biotech environment, so be prepared to discuss how you thrive in such settings. Share examples of how you've adapted to change and operated autonomously in previous roles. Show them you're not just a fit for the job, but for their culture too.