Non-clinical assessor

Non-clinical assessor

Full-Time 50000 - 65000 € / year (est.) Home office (partial)
Medicines and Healthcare Products Regulatory Agency

At a Glance

  • Tasks: Evaluate pre-clinical and environmental risks of medicinal products to support regulatory decisions.
  • Company: Leading pharmaceutical organisation based in Canary Wharf, London.
  • Benefits: Competitive salary, flexible remote work, and opportunities for professional growth.
  • Other info: Dynamic role with a mix of onsite and remote work, fostering career advancement.
  • Why this job: Make a real impact on the development of new medicines for patients.
  • Qualifications: Degree in toxicology or life sciences; experience in regulatory affairs preferred.

The predicted salary is between 50000 - 65000 € per year.

This is a full‑time, permanent opportunity based at 10 South Colonnade, Canary Wharf, London, E14 4PU. The role requires a minimum of 8 days per month onsite, up to 12 days depending on business needs, with the remainder remote.

The Non‑clinical Assessor evaluates 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.

Key Responsibilities
  • Carry out 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 protection of public health.
  • Manage own workload 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.
Qualifications
  • Degree in toxicology, ecotoxicology or another appropriate life science.
  • Previous experience in pre‑clinical, ecotoxicology or environmental regulatory affairs within the pharmaceutical industry, governmental departments or academia.
  • Up‑to‑date specialist knowledge in one or more relevant scientific areas, or broad knowledge across non‑clinical development of human medicinal products and their environmental impact.
  • Knowledge of relevant legislation and procedures applicable to licensing of human medicinal products.
  • Flexibility to adapt to changing priorities and take responsibility for achieving a successful outcome.

Non-clinical assessor employer: Medicines and Healthcare Products Regulatory Agency

As a Non-clinical Assessor at our Canary Wharf location, you will join a dynamic team dedicated to advancing public health through the evaluation of innovative medicinal products. We pride ourselves on fostering a collaborative work culture that values employee growth, offering continuous professional development opportunities and a flexible working environment that balances onsite and remote work. With a commitment to excellence and a focus on impactful contributions, we provide a rewarding career path for those passionate about making a difference in the pharmaceutical industry.

Medicines and Healthcare Products Regulatory Agency

Contact Detail:

Medicines and Healthcare Products Regulatory Agency Recruiting Team

StudySmarter Expert Advice🤫

We think this is how you could land Non-clinical assessor

Tip Number 1

Network like a pro! Reach out to professionals in the pharmaceutical industry on LinkedIn or at local events. We can’t stress enough how valuable personal connections can be in landing that Non-clinical Assessor role.

Tip Number 2

Prepare for interviews by brushing up on your knowledge of relevant legislation and procedures. We recommend creating a cheat sheet of key points to discuss, so you can impress your interviewers with your expertise!

Tip Number 3

Showcase your attention to detail! During interviews, share examples of how you've managed complex data or assessments in the past. We want to see how you can apply that skill to ensure accurate evaluations in your new role.

Tip Number 4

Don’t forget to apply through our website! It’s the best way to stay updated on the latest opportunities and ensures your application gets the attention it deserves. We’re here to help you every step of the way!

We think you need these skills to ace Non-clinical assessor

Assessment of pre-clinical data
Environmental risk evaluation
Regulatory knowledge
Toxicology
Ecotoxicology
Scientific writing
Attention to detail

Some tips for your application 🫡

Tailor Your CV:Make sure your CV highlights your relevant experience in toxicology or ecotoxicology. We want to see how your background aligns with the role of a Non-clinical Assessor, so don’t be shy about showcasing your skills!

Craft a Compelling Cover Letter:Your cover letter is your chance to shine! Use it to explain why you’re passionate about evaluating medicinal products and how your expertise can contribute to our mission. Keep it engaging and personal!

Showcase Attention to Detail:Since the role requires a high level of attention to detail, make sure your application is free from typos and errors. We appreciate precision, so double-check everything before hitting send!

Apply Through Our Website:We encourage you to apply directly through our website. It’s the best way for us to receive your application and ensures you’re considered for the role. Plus, it’s super easy!

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 the relevant legislation. Be prepared to discuss how your background aligns with the role of a Non-clinical Assessor and how you can contribute to evaluating pre-clinical data.

Showcase Your Experience

Think about specific examples from your previous roles that demonstrate your experience in pre-clinical assessments or environmental regulatory affairs. Use the STAR method (Situation, Task, Action, Result) to structure your answers and make them impactful.

Attention to Detail is Key

Since this role requires a high level of attention to detail, be ready to discuss how you ensure accuracy in your work. You might want to share any systems or processes you use to keep your data and documents organised and up-to-date.

Be Ready for Scenario Questions

Prepare for questions that ask how you would handle specific scenarios related to assessing medicinal products. Think about potential challenges you might face and how you would approach them, demonstrating your problem-solving skills and flexibility.