Senior Regulatory Medical Writer — Lead CSRs & Protocols in London
Senior Regulatory Medical Writer — Lead CSRs & Protocols

Senior Regulatory Medical Writer — Lead CSRs & Protocols in London

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

  • Tasks: Lead the creation of complex regulatory documents in a dynamic pharmaceutical environment.
  • Company: Join a leading pharmaceutical company with a focus on innovation and collaboration.
  • Benefits: Enjoy remote flexibility, competitive salary, and opportunities for professional growth.
  • Why this job: Make a significant impact in healthcare by shaping essential regulatory documents.
  • Qualifications: Advanced degree in life sciences and 4+ years in regulatory medical writing required.
  • Other info: Work remotely from the UK, Greece, Spain, or Portugal in a supportive team.

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

A leading pharmaceutical company is looking for a Senior Regulatory Medical Writer to lead the development of high-complexity regulatory documents. This full-time, permanent position offers remote flexibility within the UK, Greece, Spain or Portugal.

Candidates should have an advanced degree in life sciences and a minimum of 4 years in regulatory medical writing, including project leadership experience. The role requires excellent communication and collaboration skills to coordinate multiple teams effectively.

Senior Regulatory Medical Writer — Lead CSRs & Protocols in London employer: Fortrea

As a leading pharmaceutical company, we pride ourselves on fostering a collaborative and innovative work culture that empowers our employees to excel in their roles. With remote flexibility across the UK, Greece, Spain, and Portugal, we offer a supportive environment that prioritises work-life balance and professional growth, ensuring that our team members have access to continuous learning opportunities and the chance to lead impactful projects in regulatory medical writing.
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Contact Detail:

Fortrea Recruiting Team

StudySmarter Expert Advice 🤫

We think this is how you could land Senior Regulatory Medical Writer — Lead CSRs & Protocols in London

Tip Number 1

Network like a pro! Reach out to professionals in the pharmaceutical industry on LinkedIn or at conferences. We can’t stress enough how valuable personal connections can be in landing that Senior Regulatory Medical Writer role.

Tip Number 2

Showcase your expertise! Prepare a portfolio of your best regulatory documents and be ready to discuss them in detail during interviews. This will demonstrate your project leadership experience and communication skills, which are key for this position.

Tip Number 3

Practice makes perfect! Conduct mock interviews with friends or mentors to refine your answers and boost your confidence. We all know that first impressions count, so let’s make sure you shine!

Tip Number 4

Apply through our website! It’s the easiest way to ensure your application gets noticed. Plus, we’re always on the lookout for talented individuals like you to join our team in leading the development of high-complexity regulatory documents.

We think you need these skills to ace Senior Regulatory Medical Writer — Lead CSRs & Protocols in London

Regulatory Medical Writing
Project Leadership
Communication Skills
Collaboration Skills
Life Sciences Knowledge
Document Development
Attention to Detail
Time Management

Some tips for your application 🫡

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

Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you’re the perfect fit for this Senior Regulatory Medical Writer position. Share specific examples of your past work that demonstrate your expertise and communication skills.

Showcase Your Collaboration Skills: Since this role involves coordinating multiple teams, make sure to highlight any experiences where you successfully collaborated with others. We love seeing how you can bring people together to achieve common goals!

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 during the process!

How to prepare for a job interview at Fortrea

Know Your Regulatory Stuff

Make sure you brush up on the latest regulations and guidelines relevant to medical writing. Familiarise yourself with the specific requirements for Clinical Study Reports (CSRs) and protocols, as this will show your expertise and readiness for the role.

Showcase Your Leadership Skills

Since this position involves project leadership, be prepared to discuss your previous experiences leading teams. Have specific examples ready that highlight how you coordinated efforts, resolved conflicts, and ensured timely delivery of documents.

Communicate Clearly and Confidently

Excellent communication is key in this role. Practice articulating your thoughts clearly and concisely. During the interview, make sure to listen actively and respond thoughtfully to questions, demonstrating your collaborative spirit.

Prepare Questions for Them

Interviews are a two-way street! Prepare insightful questions about the company’s projects, team dynamics, and expectations for the role. This not only shows your interest but also helps you gauge if the company is the right fit for you.

Senior Regulatory Medical Writer — Lead CSRs & Protocols in London
Fortrea
Location: London

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  • Senior Regulatory Medical Writer — Lead CSRs & Protocols in London

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

    Fortrea

    50-100
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