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

Senior Regulatory Medical Writer — Lead CSRs & Protocols

Full-Time 42000 - 60000 £ / year (est.) No home office possible
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At a Glance

  • Tasks: Lead the creation of complex regulatory documents and coordinate with multiple teams.
  • Company: A top pharmaceutical company offering remote flexibility across several countries.
  • Benefits: Permanent position with competitive salary and remote work options.
  • Why this job: Make a significant impact in the pharmaceutical industry while working flexibly.
  • Qualifications: Advanced degree in life sciences and 4+ years in regulatory medical writing.
  • Other info: Ideal for those seeking leadership roles in a dynamic environment.

The predicted salary is between 42000 - 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 employer: Fortrea

Join a leading pharmaceutical company that values innovation and collaboration, offering a dynamic work culture where your expertise in regulatory medical writing will be recognised and rewarded. With remote flexibility across the UK, Greece, Spain, or Portugal, you will enjoy a supportive environment that fosters professional growth and development, alongside competitive benefits tailored to enhance your work-life balance.
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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

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 get your application 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

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. We love seeing your personality come through, so let us know what excites you about the role.

Showcase Your Communication Skills: Since this role involves coordinating multiple teams, it’s crucial to demonstrate your excellent communication skills. In your application, give examples of how you've successfully collaborated with others in past projects.

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 Stuff

Make sure you brush up on your knowledge of regulatory medical writing and the specific requirements for high-complexity documents. Familiarise yourself with the latest guidelines and standards in the industry, as this will show that you're not just qualified but also genuinely interested in the role.

Showcase Your Leadership Skills

Since the position involves project leadership, be ready to discuss your past experiences leading teams. Prepare specific examples where you successfully coordinated multiple teams or managed complex projects. This will demonstrate your ability to take charge and drive results.

Communication is Key

Excellent communication skills are a must for this role. Practice articulating your thoughts clearly and concisely. You might even want to prepare a few questions to ask during the interview that reflect your understanding of collaboration within teams, as this will highlight your proactive approach.

Remote Work Readiness

With remote flexibility being a part of the job, be prepared to discuss how you manage your time and stay productive while working from home. Share any tools or strategies you use to maintain effective communication and collaboration with your team, as this will reassure them of your adaptability.

Senior Regulatory Medical Writer — Lead CSRs & Protocols
Fortrea

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