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- Tasks: Assess clinical study data and provide recommendations for drug licensing.
- Company: Join the Medicines and Healthcare products Regulatory Agency (MHRA) in a dynamic role.
- Benefits: Enjoy a hybrid working model, competitive salary, and opportunities for professional growth.
- Why this job: Make a real impact on public health by promoting innovation in drug development.
- Qualifications: MSc or PhD in statistics or related field; relevant experience required.
- Other info: Collaborate with medical experts and advisory committees in a supportive environment.
The predicted salary is between 36000 - 60000 £ per year.
Location: 10 South Colonnade, Canary Wharf London, E14 4PU. This full‑time, permanent position is part of the Medicines and Healthcare products Regulatory Agency (MHRA). We are implementing a hybrid working model with at least 8 days per month in the office.
As part of the evaluation of data submitted for product licensing, you will assess clinical study designs and statistical analysis methods, critically interpret results, and advise on good drug development. You will report to the Statistics Team Lead in Innovative Medicines and collaborate with medical colleagues, advisory committees and company representatives.
Key responsibilities:
- Carry out assessments of clinical study data in marketing authorisation applications and early access to medicine scheme applications, providing recommendations aligned to public health protection.
- Provide timely and appropriate scientific and regulatory advice in line with contemporary guidance, promoting innovation while protecting public health.
- Prepare and present objective assessments or scientific papers at advisory groups such as the Commission on Human Medicines.
- Review protocols for clinical investigations planned to be run in the UK.
Qualifications and experience:
- MSc or PhD in statistics or a related subject, or equivalent experience.
- Relevant work experience and knowledge in design, analysis and interpretation of clinical studies.
- Excellent written and verbal communication skills, with the ability to produce authoritative reports and deliver presentations.
- Knowledge of relevant guidelines, regulations and procedures, or the ability to acquire such knowledge quickly.
- Ability to work under pressure, meet tight timelines and prioritise work.
Person specification:
- Communicating and influencing: Excellent written and verbal communication; ability to write authoritative reports and present to target audiences.
- Delivering at pace: Ability to work under pressure, meet tight timelines and prioritise work.
- Working together: Evidence of effective interpersonal skills in a range of situations.
- Experience: Relevant work experience and knowledge relating to design, analysis and interpretation of clinical studies.
- Education: MSc or PhD in statistics or a closely related subject, or equivalent experience.
- Technical: Knowledge of guidelines, regulations and procedures, or quick learning ability; IT skills appropriate for an information-based organisation.
How to apply: Send your CV and a cover letter to careers@mhra.gov.uk or apply via the online form. The selection process includes an online application, interview and presentation.
EEO MHRA is an equal opportunity employer and values diversity.
Statistical Assessor employer: 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 Statistical Assessor
✨Tip Number 1
Network like a pro! Reach out to professionals in the field of statistics and drug development. Attend industry events or webinars, and don’t be shy about asking for informational interviews. We all know that sometimes it’s not just what you know, but who you know!
✨Tip Number 2
Prepare for your interview by brushing up on your knowledge of clinical study designs and statistical analysis methods. We recommend practising common interview questions and even presenting your own assessments. This will show your potential employer that you’re ready to hit the ground running!
✨Tip Number 3
Don’t forget to showcase your communication skills! Whether it’s through your presentation during the interview or your ability to explain complex concepts simply, we want to see how well you can convey your ideas. Remember, you’ll be advising on good drug development, so clarity is key!
✨Tip Number 4
Apply through our website! It’s the easiest way to ensure your application gets noticed. Plus, you’ll have access to all the latest job openings and updates directly from us. Let’s make sure your application stands out!
We think you need these skills to ace Statistical Assessor
Some tips for your application 🫡
Tailor Your CV: Make sure your CV is tailored to the Statistical Assessor role. Highlight your relevant experience in clinical study design and statistical analysis, and don’t forget to showcase your excellent communication skills!
Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you’re passionate about the role and how your background aligns with the responsibilities outlined in the job description. Keep it concise but impactful.
Showcase Your Technical Skills: Since this role requires knowledge of guidelines and regulations, be sure to mention any relevant technical skills or experiences. If you’ve worked under pressure or met tight deadlines, share those examples too!
Apply Through Our Website: We encourage you to apply through our website for a smoother application process. It’s the best way to ensure your application gets the attention it deserves. Good luck!
How to prepare for a job interview at Medicines and Healthcare Products Regulatory Agency
✨Know Your Stats
Brush up on your statistical knowledge and be ready to discuss clinical study designs and analysis methods. Make sure you can explain how you would assess data and provide recommendations, as this will likely come up during the interview.
✨Prepare for Presentations
Since you'll need to present objective assessments, practice delivering your findings clearly and confidently. Use examples from your past work to illustrate your points, and be prepared to answer questions about your methodology and conclusions.
✨Understand the Regulatory Landscape
Familiarise yourself with the relevant guidelines and regulations that govern drug development and clinical studies. This knowledge will not only help you in the interview but also show that you're serious about the role and understand its importance.
✨Showcase Your Communication Skills
Highlight your ability to communicate complex information effectively. Be ready to discuss how you've written authoritative reports or presented to diverse audiences in the past, as strong communication is key for this position.
