Lead Medical Writer, Regulatory & CTD Expert
Lead Medical Writer, Regulatory & CTD Expert

Lead Medical Writer, Regulatory & CTD Expert

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

  • Tasks: Prepare clinical documents and lead writing projects in a dynamic environment.
  • Company: A leading clinical research organisation dedicated to improving patient outcomes.
  • Benefits: Competitive salary, mentorship opportunities, and a chance to make a global impact.
  • Why this job: Join a mission-driven team and enhance your skills while helping patients worldwide.
  • Qualifications: Bachelor's in life sciences; Master's or Ph.D. preferred with 7+ years of experience.
  • Other info: Mentorship role with opportunities for professional growth and development.

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

A leading clinical research organization is looking for a Lead Medical Writer in Greater London. This role involves preparing clinical documents per regulatory standards, leading writing projects, and mentoring junior staff.

Candidates should possess a Bachelor's Degree in life sciences, with a preferred Master's or Ph.D., and have at least 7 years of relevant experience. Excellent communication, organizational, and negotiation skills are essential for success in this position.

Join a company committed to improving patient outcomes worldwide.

Lead Medical Writer, Regulatory & CTD Expert employer: IQVIA

As a leading clinical research organization based in Greater London, we pride ourselves on fostering a collaborative and innovative work culture that prioritises employee growth and development. Our commitment to improving patient outcomes is matched by our dedication to providing comprehensive benefits, mentorship opportunities, and a supportive environment where your expertise as a Lead Medical Writer can truly make a difference.
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Contact Detail:

IQVIA Recruiting Team

StudySmarter Expert Advice 🤫

We think this is how you could land Lead Medical Writer, Regulatory & CTD Expert

✨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 lead to job opportunities that aren’t even advertised.

✨Tip Number 2

Showcase your expertise! When you get the chance to chat with potential employers, highlight your experience in preparing clinical documents and leading projects. We want to see how you can bring value to their team.

✨Tip Number 3

Practice makes perfect! Before any interviews, we recommend doing mock interviews with friends or mentors. This will help you articulate your skills and experiences clearly, especially your communication and negotiation skills.

✨Tip Number 4

Apply through our website! It’s the best way to ensure your application gets noticed. Plus, we’re always looking for passionate individuals who are committed to improving patient outcomes, just like you!

We think you need these skills to ace Lead Medical Writer, Regulatory & CTD Expert

Clinical Document Preparation
Regulatory Standards Knowledge
Project Leadership
Mentoring Skills
Bachelor's Degree in Life Sciences
Master's or Ph.D. (preferred)
7+ Years of Relevant Experience
Excellent Communication Skills
Organisational Skills
Negotiation Skills

Some tips for your application 🫡

Tailor Your CV: Make sure your CV highlights your relevant experience in medical writing and regulatory standards. 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 improving patient outcomes and how your expertise can contribute to our mission. Keep it engaging and personal.

Showcase Your Communication Skills: As a Lead Medical Writer, communication is key. In your application, demonstrate your ability to convey complex information clearly and concisely. We love seeing examples of your writing style!

Apply Through Our Website: We encourage you to apply directly through our website for a smoother process. It helps us keep track of applications and ensures you don’t miss out on any important updates from us!

How to prepare for a job interview at IQVIA

✨Know Your Regulatory Standards

Make sure you brush up on the latest regulatory standards relevant to clinical documents. Familiarise yourself with guidelines from agencies like the FDA and EMA, as this will show your expertise and commitment to quality in your writing.

✨Showcase Your Leadership Skills

Since this role involves leading writing projects and mentoring junior staff, be prepared to discuss your previous leadership experiences. Share specific examples of how you've guided teams or improved processes in past roles to demonstrate your capability.

✨Prepare for Technical Questions

Expect technical questions related to medical writing and the Clinical Trial Document (CTD) format. Review common challenges faced in this area and think about how you would address them. This will help you articulate your problem-solving skills during the interview.

✨Communicate Clearly and Confidently

Excellent communication is key for this position. Practice articulating your thoughts clearly and confidently. Consider doing mock interviews with a friend or colleague to refine your delivery and ensure you convey your ideas effectively.

Lead Medical Writer, Regulatory & CTD Expert
IQVIA
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  • Lead Medical Writer, Regulatory & CTD Expert

    Full-Time
    48000 - 72000 £ / year (est.)
  • I

    IQVIA

    10000+
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