Clinical Statistics Assessor - Drug Evaluation in London
Clinical Statistics Assessor - Drug Evaluation

Clinical Statistics Assessor - Drug Evaluation in London

London Full-Time 36000 - 60000 £ / year (est.) No home office possible
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At a Glance

  • Tasks: Assess clinical study designs and provide regulatory advice for drug evaluation.
  • Company: Reputable healthcare regulatory agency in the UK.
  • Benefits: Hybrid working model, competitive salary, and professional development opportunities.
  • Why this job: Make a real impact in healthcare by evaluating data for product licensing.
  • Qualifications: MSc or PhD in statistics or related field with relevant work experience.
  • Other info: Excellent communication skills required; at least 8 days in the office monthly.

The predicted salary is between 36000 - 60000 £ per year.

A healthcare regulatory agency in the UK is seeking a qualified professional to assess clinical study designs and provide regulatory advice. The role involves evaluating data for product licensing and preparing reports for advisory committees.

Ideal candidates should hold an MSc or PhD in statistics or a related field, possess relevant work experience, and have excellent communication skills.

This full-time position offers a hybrid working model and requires at least 8 days per month in the office.

Clinical Statistics Assessor - Drug Evaluation in London employer: Mhra

As a leading healthcare regulatory agency in the UK, we pride ourselves on fostering a collaborative and innovative work culture that empowers our employees to make a meaningful impact in public health. With a strong commitment to professional development, we offer numerous growth opportunities and a hybrid working model that promotes work-life balance, making us an excellent employer for those passionate about advancing drug evaluation and regulatory science.
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Contact Detail:

Mhra Recruiting Team

StudySmarter Expert Advice 🤫

We think this is how you could land Clinical Statistics Assessor - Drug Evaluation in London

✨Tip Number 1

Network like a pro! Reach out to professionals in the healthcare regulatory 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 clinical study designs and regulatory processes. 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 communication skills! During interviews, make sure to articulate your thoughts clearly and concisely. We know it can be nerve-wracking, but remember, they want to see how you present your ideas.

✨Tip Number 4

Don’t forget to apply through our website! It’s the best way to ensure your application gets noticed. Plus, we often have exclusive roles listed there that you won’t find anywhere else.

We think you need these skills to ace Clinical Statistics Assessor - Drug Evaluation in London

Clinical Study Design Assessment
Regulatory Advice
Data Evaluation
Product Licensing
Report Preparation
MSc or PhD in Statistics
Relevant Work Experience
Communication Skills

Some tips for your application 🫡

Tailor Your CV: Make sure your CV highlights your MSc or PhD in statistics and any relevant work experience. We want to see how your background aligns with the role, 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 clinical study designs and how your expertise can contribute to our team. Keep it engaging and professional.

Show Off Your Communication Skills: Since excellent communication is key for this role, make sure your application reflects that. Use clear and concise language, and don’t forget to proofread for any typos or errors 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 position. Plus, it’s super easy!

How to prepare for a job interview at Mhra

✨Know Your Stats

Brush up on your statistical knowledge and be ready to discuss specific methodologies relevant to clinical study designs. Familiarise yourself with common statistical software used in the industry, as you might be asked about your experience with them.

✨Understand Regulatory Frameworks

Make sure you have a solid grasp of the regulatory guidelines that govern drug evaluation in the UK. Being able to articulate how these regulations impact clinical studies will show that you’re not just knowledgeable but also proactive in understanding the field.

✨Prepare for Scenario Questions

Expect to face scenario-based questions where you’ll need to evaluate hypothetical clinical data or study designs. Practise articulating your thought process clearly, as this will demonstrate your analytical skills and ability to provide sound regulatory advice.

✨Showcase Your Communication Skills

Since excellent communication is key for this role, prepare to discuss how you've effectively communicated complex statistical concepts to non-experts in the past. Use examples from your experience to illustrate your ability to convey information clearly and concisely.

Clinical Statistics Assessor - Drug Evaluation in London
Mhra
Location: London

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  • Clinical Statistics Assessor - Drug Evaluation in London

    London
    Full-Time
    36000 - 60000 £ / year (est.)
  • M

    Mhra

    500-1000
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