At a Glance
- Tasks: Evaluate pre-clinical and environmental risks of innovative medicines to support regulatory decisions.
- Company: Join the Medicines and Healthcare products Regulatory Agency, enhancing public health daily.
- Benefits: Flexible hybrid working, competitive salary, and opportunities for professional growth.
- Other info: Dynamic role with excellent career progression in a supportive environment.
- Why this job: Make a real impact on healthcare by assessing groundbreaking medicinal products.
- Qualifications: Degree in toxicology or life sciences; experience in regulatory affairs preferred.
The predicted salary is between 40000 - 50000 € per year.
This is a full-time opportunity, on a permanent basis. The role will be based in 10 South Colonnade, Canary Wharf London, E14 4PU. Government departments and agencies are working towards implementing a minimum 60% attendance in office sites. We are currently implementing a flexible, hybrid way of working, with a minimum of 8 days per month working on site to enable the collaboration and contact with partners and stakeholders needed to deliver MHRA business. Attendance on site is driven by business needs so depending on the nature of the role, this can flex up to 12 days a month, with the remainder of time worked either remotely or in the office. Some roles will need to be on site more regularly.
Who are we? The Medicines and Healthcare products Regulatory Agency enhance and improve the health of millions of people every day through the effective regulation of medicines and medical devices, underpinned by science and research. The objective of the Healthcare Quality and Access portfolio is to drive quality and critically appraise benefits and risks to inform robust decisions on healthcare access including accelerated access pathways. It will do this by bringing together a fusion of our capabilities across both medicines and medical devices to enable licensing and market access, as well as ensuring compliance with regulations and standards.
The Innovative Medicines function delivers a risk appropriate critical appraisal of quality, safety and efficacy of innovative medicinal products, determining whether a product’s benefits outweighs the risks. It aims to accelerate their route to market to drive earlier patient access. Through this function the Agency will be seen as a leader in facilitating early access to safe and innovative medicines attracting the life sciences sector and contributing to a positive patient experience and to the improvement of public health outcomes.
What’s the role? The Non-clinical Assessor evaluates the pre-clinical and environmental risk aspects of medicinal products to support regulatory decisions on clinical trials and marketing authorisations. The role involves assessing innovative chemical and biological products and providing expert recommendations that influence the development and availability of new medicines for patients.
- Carry out the assessment of pre-clinical data and/or environmental risk aspects provided in marketing authorisation applications and clinical trial authorisations for chemical and biological products making appropriate recommendations and decisions in line with the protection of public health.
- Manage own workload working in conjunction with service coordinators and other assessors to meet agency deadlines.
- Prepare and present objective assessments or other scientific papers to expert advisory bodies.
- Display a high level of attention to detail to ensure up to date accurate data and documents are held on internal databases.
Who are we looking for? Our successful candidate will demonstrate the following:
- Degree in toxicology, ecotoxicology or other appropriate life science.
- Previous experience in one of the following: pre-clinical, ecotoxicology or environmental regulatory affairs within the pharmaceutical industry, governmental departments or academia.
- Up to date specialist level of knowledge in one or more relevant scientific areas or broader knowledge across the range of scientific activities in relation to the non-clinical development of human medicinal products and their environmental impact.
- Knowledge of relevant legislation and procedures applicable to the licensing of human medicinal products.
- Flexibility to adapt to changing priorities and take responsibility for achieving a successful outcome.
Person Specification:
- Delivering at Pace: Flexibility to adapt to changing priorities and take responsibility for achieving a successful outcome.
- Communicating and Influencing: Excellent written and verbal communication skills.
- Managing a Quality Service: Ability to handle throughput of work commensurate with experience and knowledge to meet required deadlines.
- Making effective decisions: Evidence of applying scientific perspective to data evaluations and advise others.
Experience Criteria:
- Previous experience in one of the following; pre-clinical, ecotoxicology or environmental regulatory affairs within the pharmaceutical industry, governmental departments or academia.
- Experience with data analysis, risk assessment methodologies and/or regulatory frameworks.
Technical Criteria:
- Up to date specialist level of knowledge in one or more relevant scientific areas or broader knowledge across the range of scientific activities in relation to the non-clinical development of human medicinal products and their environmental impact.
- Sound knowledge of relevant legislation and procedures applicable to the licensing of human medicinal products.
- Degree in toxicology, ecotoxicology or other appropriate life science.
If you would like to find out more about this fantastic opportunity, please read our Job Description and Person Specification!
Closing date: 31st May 2026
Shortlisting date: from 1st June 2026
Interview date: week commencing 29th June 2026
Non-clinical assessor in London employer: Medicines and Healthcare Products Regulatory Agency
The Medicines and Healthcare products Regulatory Agency (MHRA) is an exceptional employer, offering a dynamic work environment in the heart of Canary Wharf, London. With a commitment to flexible hybrid working, employees enjoy a balance between collaboration on-site and remote work, fostering a culture of innovation and professional growth. The agency prioritises employee development through continuous training opportunities, while contributing to public health by regulating medicines and medical devices that enhance the lives of millions.
Contact Detail:
Medicines and Healthcare Products Regulatory Agency Recruiting Team
StudySmarter Expert Advice🤫
We think this is how you could land Non-clinical assessor in London
✨Tip Number 1
Network like a pro! Reach out to people in the industry, especially those who work at the MHRA or similar organisations. A friendly chat can open doors and give you insights that might just help you stand out.
✨Tip Number 2
Prepare for your interview by diving deep into the role's specifics. Brush up on your knowledge of environmental risk assessments and relevant legislation. The more you know, the more confident you'll feel when discussing your expertise!
✨Tip Number 3
Practice makes perfect! Get a mate to do a mock interview with you. This will help you articulate your thoughts clearly and get comfortable with the types of questions you might face.
✨Tip Number 4
Don't forget to apply through our website! It’s the best way to ensure your application gets the attention it deserves. Plus, you’ll find all the info you need about the role right there.
We think you need these skills to ace Non-clinical assessor in London
Some tips for your application 🫡
Read the Job Description Carefully:Before you start your application, make sure to read the job description thoroughly. It’s packed with details about what we’re looking for, and tailoring your application to match those requirements can really make you stand out!
Be Specific in Your Examples:When answering competency-based questions, use specific examples from your experience that demonstrate your skills. We want to see how you've tackled challenges in the past, so don’t hold back on the details!
Check Your Work:Attention to detail is key! Before submitting your application, double-check for any typos or errors. A polished application shows us that you care about quality and professionalism.
Apply Through Our Website:Make sure to submit your application through our website. It’s the best way to ensure it gets to us directly, and you’ll find all the necessary forms and information there to help you along the way!
How to prepare for a job interview at Medicines and Healthcare Products Regulatory Agency
✨Know Your Stuff
Make sure you brush up on your knowledge of toxicology, ecotoxicology, and relevant legislation. The interviewers will likely ask you about your experience with pre-clinical data and environmental risk assessments, so be ready to discuss specific examples from your past work.
✨Showcase Your Communication Skills
As a Non-clinical Assessor, you'll need to present objective assessments clearly. Practice explaining complex scientific concepts in simple terms. This will not only help you in the interview but also demonstrate your ability to communicate effectively with stakeholders.
✨Prepare for Behavioural Questions
Expect questions that assess your flexibility and decision-making skills. Think of situations where you've had to adapt to changing priorities or make tough decisions based on scientific data. Use the STAR method (Situation, Task, Action, Result) to structure your answers.
✨Get Ready for the Presentation
You'll need to prepare a presentation as part of your interview. Choose a topic related to environmental risk assessments or regulatory frameworks that you're passionate about. Make it engaging and informative, and practice delivering it to ensure you're confident on the day.
