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- Tasks: Create and edit regulatory documents for global submissions in a collaborative team.
- Company: Join a leading global medical communications agency making a real impact in healthcare.
- Benefits: Enjoy remote work flexibility, structured career development, and excellent support systems.
- Why this job: Be part of a high-impact role that values collaboration and professionalism while contributing to meaningful projects.
- Qualifications: Previous experience in regulatory writing within medical communications or pharmaceuticals is essential.
- Other info: Work across multiple projects while maintaining high standards and meeting deadlines.
The predicted salary is between 36000 - 60000 £ per year.
We are currently partnering with a leading global medical communications agency to support their search for an experienced Regulatory Medical Writer. This is a fantastic opportunity to contribute to meaningful regulatory submissions across a variety of therapeutic areas, working with a highly collaborative and well-established team.
This position involves the development of high-quality, accurate, and compliant documentation to support global regulatory submissions. You will work closely with internal teams and external clients to ensure that deliverables meet both scientific and regulatory standards.
- Write and edit a variety of regulatory documents, ensuring all documents are clear, accurate, and aligned with relevant regulatory guidelines and client expectations.
- Review and quality-check clinical documentation, data outputs, and other supporting materials.
- Liaise with client teams to manage timelines, address queries, and resolve content or compliance issues.
- Conduct background research to confirm references and stay aligned with current regulatory requirements.
- Work across multiple projects while maintaining high standards and meeting deadlines.
Previous experience producing regulatory documentation within a medical communications agency or pharmaceutical environment is required. A strong understanding of regulatory writing standards and processes is essential, including experience with reviewing protocols, statistical analysis plans, and clinical data.
This role offers the opportunity to work in a high-impact environment with a global client base, excellent support systems, and the ability to work remotely or flexibly. You will also benefit from structured career development, internal training, and a strong culture of collaboration and professionalism.
Writer (Remote) employer: Meet Life Sciences
Contact Detail:
Meet Life Sciences Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Writer (Remote)
✨Tip Number 1
Familiarise yourself with the latest regulatory guidelines and standards in medical writing. This will not only help you understand the expectations of the role but also demonstrate your commitment to staying updated in a fast-evolving field.
✨Tip Number 2
Network with professionals in the medical communications and pharmaceutical industries. Engaging with others in the field can provide valuable insights and potentially lead to referrals or recommendations for the position.
✨Tip Number 3
Prepare to discuss specific examples of your previous work with regulatory documents during interviews. Highlighting your experience with various therapeutic areas and your ability to manage multiple projects will set you apart from other candidates.
✨Tip Number 4
Showcase your collaborative skills by discussing how you've successfully worked with cross-functional teams in the past. Emphasising your ability to liaise effectively with clients and internal teams will align well with the job's requirements.
We think you need these skills to ace Writer (Remote)
Some tips for your application 🫡
Understand the Role: Before applying, make sure you fully understand the responsibilities and requirements of a Regulatory Medical Writer. Familiarise yourself with the types of documents you'll be expected to write and the regulatory standards involved.
Tailor Your CV: Highlight your relevant experience in regulatory writing, especially within medical communications or pharmaceutical environments. Be specific about the types of documents you've worked on and any regulatory guidelines you are familiar with.
Craft a Compelling Cover Letter: Use your cover letter to showcase your passion for regulatory writing and your understanding of the role. Mention specific projects or experiences that demonstrate your ability to produce high-quality documentation and work collaboratively.
Proofread Your Application: Ensure that your CV and cover letter are free from errors. Given the nature of the role, attention to detail is crucial. Consider asking a colleague or friend to review your application before submission.
How to prepare for a job interview at Meet Life Sciences
✨Showcase Your Regulatory Knowledge
Make sure to highlight your understanding of regulatory writing standards and processes during the interview. Be prepared to discuss specific examples from your previous experience that demonstrate your ability to produce high-quality regulatory documentation.
✨Prepare for Technical Questions
Expect questions related to clinical documentation, data outputs, and compliance issues. Brush up on relevant guidelines and be ready to explain how you ensure accuracy and clarity in your writing.
✨Demonstrate Collaboration Skills
Since this role involves working closely with internal teams and external clients, be ready to share examples of how you've successfully collaborated in the past. Highlight your communication skills and ability to manage timelines effectively.
✨Research the Company and Its Clients
Familiarise yourself with the medical communications agency and its client base. Understanding their therapeutic areas and recent projects can help you tailor your responses and show genuine interest in the role.
