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

Lead Medical Writer, Regulatory & CTD Expert in London

London Full-Time 48000 - 72000 £ / year (est.) No home office possible
Go Premium
I

At a Glance

  • Tasks: Prepare clinical documents and lead writing projects while mentoring junior staff.
  • Company: A leading clinical research organisation dedicated to improving patient outcomes.
  • Benefits: Competitive salary, professional development, and a chance to make a global impact.
  • Why this job: Join a mission-driven team and enhance your skills in a vital industry.
  • Qualifications: Bachelor's in life sciences; Master's or Ph.D. preferred with 7 years of experience.
  • Other info: Dynamic work environment with opportunities for career advancement.

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 in London 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.
I

Contact Detail:

IQVIA Recruiting Team

StudySmarter Expert Advice 🤫

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

✨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 you.

✨Tip Number 2

Showcase your expertise! Prepare a portfolio of your best writing samples and be ready to discuss them in detail. This is your chance to shine and demonstrate your skills as a Lead Medical Writer.

✨Tip Number 3

Practice makes perfect! Conduct mock interviews with friends or mentors to refine your answers, especially around your experience in regulatory standards and mentoring. We want you to feel confident when it’s your turn!

✨Tip Number 4

Apply through our website! It’s the easiest way to ensure your application gets noticed. Plus, we love seeing candidates who take the initiative to connect directly with us.

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

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 this role and how your expertise can contribute to our mission of improving patient outcomes. 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 and clarity!

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 get the best chance to join our team at StudySmarter!

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. Being able to discuss these confidently will show that you’re not just familiar with the basics, but that you’re also up-to-date and ready to lead writing projects.

✨Showcase Your Leadership Skills

Since this role involves mentoring junior staff, be prepared to share examples of how you've successfully led teams or projects in the past. Highlight your ability to guide others and foster a collaborative environment.

✨Communicate Clearly and Effectively

Excellent communication is key for this position. Practice articulating your thoughts clearly and concisely. You might even want to prepare a few examples of complex information you've simplified for different audiences.

✨Prepare Questions About Patient Outcomes

Since the company is committed to improving patient outcomes, come prepared with insightful questions about their initiatives. This shows your genuine interest in their mission and how you can contribute to it.

Lead Medical Writer, Regulatory & CTD Expert in London
IQVIA
Location: London
Go Premium

Land your dream job quicker with Premium

You’re marked as a top applicant with our partner companies
Individual CV and cover letter feedback including tailoring to specific job roles
Be among the first applications for new jobs with our AI application
1:1 support and career advice from our career coaches
Go Premium

Money-back if you don't land a job in 6-months

I
  • Lead Medical Writer, Regulatory & CTD Expert in London

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

    IQVIA

    10000+
Similar positions in other companies
UK’s top job board for Gen Z
discover-jobs-cta
Discover now
>