Senior Medical Writer: Regulatory & Clinical Docs in London
Senior Medical Writer: Regulatory & Clinical Docs

Senior Medical Writer: Regulatory & Clinical Docs in London

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

  • Tasks: Draft clinical study documents and manage project timelines in a dynamic environment.
  • Company: Global biotechnology company focused on advancing human health.
  • Benefits: Competitive salary, health benefits, and opportunities for professional growth.
  • Why this job: Join a team dedicated to innovative science and make a real impact on health.
  • Qualifications: Bachelor’s degree and experience in medical writing with project management skills.
  • Other info: Collaborate with cross-functional teams to ensure regulatory compliance.

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

A global biotechnology company is seeking a Senior Medical Writer to draft clinical study documents and manage project timelines. This role involves collaborating with cross-functional teams to ensure regulatory compliance and effective communication of complex scientific concepts.

Candidates should have a Bachelor’s degree and experience in medical writing, along with advanced skills in project management and regulatory requirements.

Join a team dedicated to advancing human health through innovative science.

Senior Medical Writer: Regulatory & Clinical Docs in London employer: BioMarin Pharmaceutical Inc.

As a leading global biotechnology company, we pride ourselves on fostering a collaborative and innovative work culture that empowers our employees to make a meaningful impact on human health. Our commitment to professional development is evident through tailored growth opportunities and continuous learning initiatives, ensuring that our team members thrive in their careers. Located in a vibrant area, we offer competitive benefits and a supportive environment that values diversity and encourages creative thinking.
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Contact Detail:

BioMarin Pharmaceutical Inc. Recruiting Team

StudySmarter Expert Advice 🤫

We think this is how you could land Senior Medical Writer: Regulatory & Clinical Docs in London

✨Tip Number 1

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

✨Tip Number 2

Showcase your expertise! Prepare a portfolio of your best clinical study documents and project management examples. When you get that interview, we want you to wow them with your skills and experience.

✨Tip Number 3

Practice makes perfect! Conduct mock interviews with friends or mentors to refine your answers, especially around regulatory compliance and scientific communication. We want you to feel confident and ready to impress.

✨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 eager to contribute to advancing human health through innovative science.

We think you need these skills to ace Senior Medical Writer: Regulatory & Clinical Docs in London

Medical Writing
Regulatory Compliance
Project Management
Collaboration
Communication Skills
Scientific Concept Communication
Attention to Detail
Time Management
Cross-Functional Teamwork
Bachelor’s Degree in a Relevant Field

Some tips for your application 🫡

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

Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you’re passionate about advancing human health and how your background makes you a perfect fit for our team. Keep it concise but impactful!

Showcase Your Collaboration Skills: Since this role involves working with cross-functional teams, make sure to mention any experiences where you’ve successfully collaborated with others. We love seeing teamwork in action!

Apply Through Our Website: We encourage you to apply directly through our website. It’s the best way to ensure your application gets into the right hands. Plus, it shows us you’re genuinely interested in joining our innovative team!

How to prepare for a job interview at BioMarin Pharmaceutical Inc.

✨Know Your Stuff

Make sure you brush up on your medical writing skills and regulatory knowledge. Familiarise yourself with the types of clinical study documents you'll be drafting, as well as the latest guidelines from regulatory bodies. This will show that you're not just qualified but also genuinely interested in the role.

✨Showcase Your Project Management Skills

Since this role involves managing project timelines, be ready to discuss your experience with project management. Prepare specific examples of how you've successfully managed projects in the past, including any tools or methodologies you used to keep everything on track.

✨Collaboration is Key

This position requires working with cross-functional teams, so highlight your teamwork skills. Think of instances where you've collaborated with different departments or stakeholders to achieve a common goal. Be prepared to discuss how you handle conflicts and ensure effective communication.

✨Communicate Complex Concepts Clearly

As a Senior Medical Writer, you'll need to convey complex scientific ideas in an understandable way. Practice explaining some intricate concepts in simple terms. This will demonstrate your ability to communicate effectively, which is crucial for the role.

Senior Medical Writer: Regulatory & Clinical Docs in London
BioMarin Pharmaceutical Inc.
Location: London
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