Principal Regulatory Medical Writer — Clinical Submissions Lead
Principal Regulatory Medical Writer — Clinical Submissions Lead

Principal Regulatory Medical Writer — Clinical Submissions Lead

Full-Time 48000 - 72000 £ / year (est.) No home office possible
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At a Glance

  • Tasks: Lead the creation of high-quality regulatory and clinical documents in a collaborative environment.
  • Company: A top clinical research organisation in the UK with a focus on innovation.
  • Benefits: Competitive salary, comprehensive benefits, and a strong emphasis on work-life balance.
  • Why this job: Make a significant impact in the medical field while enjoying a supportive work culture.
  • Qualifications: Extensive experience in medical writing, especially with regulatory submissions.
  • Other info: Join a dynamic team dedicated to advancing healthcare solutions.

The predicted salary is between 48000 - 72000 £ per year.

A leading clinical research organization in the UK is seeking a Principal Medical Writer to lead the development of high-quality regulatory and clinical documents. You will work closely with cross-functional teams, ensuring compliance with industry standards.

Ideal candidates will have significant experience in medical writing, particularly with regulatory submissions. This position offers competitive salary and comprehensive benefits, focused on well-being and work-life balance for you and your family.

Principal Regulatory Medical Writer — Clinical Submissions Lead employer: ICON Strategic Solutions

As a leading clinical research organisation in the UK, we pride ourselves on fostering a collaborative and innovative work culture that prioritises employee well-being and professional growth. Our Principal Regulatory Medical Writers enjoy competitive salaries, comprehensive benefits, and a strong emphasis on work-life balance, making it an ideal environment for those seeking meaningful and rewarding careers in medical writing.
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Contact Detail:

ICON Strategic Solutions Recruiting Team

StudySmarter Expert Advice 🤫

We think this is how you could land Principal Regulatory Medical Writer — Clinical Submissions Lead

Tip Number 1

Network like a pro! Reach out to professionals in the clinical research field on LinkedIn or at industry events. We can’t stress enough how personal connections can open doors for us.

Tip Number 2

Prepare for interviews by practising common questions and scenarios related to regulatory submissions. We should also be ready to showcase our writing samples that highlight our expertise in medical writing.

Tip Number 3

Don’t just apply anywhere; focus on organisations that align with your values and career goals. We recommend checking out opportunities directly on our website for the best fit!

Tip Number 4

Follow up after interviews! A simple thank-you email can set us apart from other candidates. It shows our enthusiasm and professionalism, which is key in the regulatory writing space.

We think you need these skills to ace Principal Regulatory Medical Writer — Clinical Submissions Lead

Medical Writing
Regulatory Submissions
Cross-Functional Collaboration
Compliance with Industry Standards
Attention to Detail
Project Management
Communication Skills
Experience in Clinical Research

Some tips for your application 🫡

Tailor Your CV: Make sure your CV highlights your experience in medical writing and regulatory submissions. We want to see how your skills align with the role, so don’t be shy about showcasing your achievements!

Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you’re the perfect fit for the Principal Regulatory Medical Writer position. We love seeing passion and personality, so let us know what excites you about this opportunity.

Showcase Your Teamwork Skills: Since you'll be working closely with cross-functional teams, highlight any relevant experiences where you've collaborated effectively. We value teamwork, so share examples that demonstrate your ability to work well with others.

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 don’t miss out on any important updates. Plus, we love seeing applications come in through our own platform!

How to prepare for a job interview at ICON Strategic Solutions

Know Your Stuff

Make sure you brush up on your medical writing knowledge, especially around regulatory submissions. Familiarise yourself with the latest industry standards and guidelines, as this will show that you're not just experienced but also current in your field.

Showcase Your Experience

Prepare specific examples from your past work that highlight your expertise in leading the development of clinical documents. Be ready to discuss challenges you've faced and how you overcame them, as this demonstrates your problem-solving skills and leadership abilities.

Understand the Company Culture

Research the clinical research organisation and its values. Knowing their focus on well-being and work-life balance can help you tailor your responses to align with their culture, showing that you’re a good fit for the team.

Ask Insightful Questions

Prepare thoughtful questions about the role and the team dynamics. This not only shows your interest in the position but also gives you a chance to assess if the company aligns with your career goals and values.

Principal Regulatory Medical Writer — Clinical Submissions Lead
ICON Strategic Solutions

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