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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 a supportive team culture.
- Why this job: Contribute to meaningful projects while developing your skills in a high-impact environment.
- Qualifications: Life sciences degree preferred; experience in regulatory writing is a plus.
- Other info: This is an entry-level, part-time role perfect for students looking to gain valuable experience.
Regulatory Writer – Remote – Studentjob.co.uk
Regulatory Writer – Remote – Studentjob.co.uk
2 days ago Be among the first 25 applicants
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.
About the Role:
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.
Key Responsibilities:
- Write and edit a variety of regulatory documents (e.g., clinical study reports, protocols, CTD clinical summaries, investigator brochures) across multiple therapeutic areas
- Ensure 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
Requirements:
- Previous experience producing regulatory documentation within a medical communications agency or pharmaceutical environment
- Strong understanding of regulatory writing standards and processes (e.g., ICH, GCP)
- Life sciences degree (advanced degree preferred)
- High attention to detail, critical thinking, and the ability to work independently or as part of a team
- Experience with reviewing protocols, statistical analysis plans, and clinical data
- Excellent verbal and written communication skills
What’s on Offer:
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.
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Regulatory Writer - Remote - Studentjob.co.uk employer: Jobster
Contact Detail:
Jobster Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Regulatory Writer - Remote - Studentjob.co.uk
✨Tip Number 1
Familiarise yourself with the latest regulatory guidelines and standards, such as ICH and GCP. This knowledge will not only boost your confidence but also demonstrate your commitment to staying updated in the field.
✨Tip Number 2
Network with professionals in the medical communications and pharmaceutical industries. Attend relevant webinars or join online forums to connect with others who can provide insights or even refer you to opportunities.
✨Tip Number 3
Prepare to discuss specific examples of your previous regulatory writing experience during interviews. Highlight how you ensured compliance and quality in your documentation, as this will showcase your expertise.
✨Tip Number 4
Demonstrate your ability to work collaboratively by sharing experiences where you successfully liaised with teams or clients. This is crucial for a role that involves working closely with various stakeholders.
We think you need these skills to ace Regulatory Writer - Remote - Studentjob.co.uk
Some tips for your application 🫡
Understand the Role: Before applying, make sure you fully understand the responsibilities of a Regulatory Writer. Familiarise yourself with the types of documents you'll be writing and the regulatory standards involved.
Tailor Your CV: Highlight your relevant experience in regulatory writing or medical communications. Be specific about the types of documents you've worked on and any regulatory guidelines you're familiar with, such as ICH or GCP.
Craft a Compelling Cover Letter: Use your cover letter to showcase your passion for regulatory writing and your understanding of the role. Mention specific experiences that demonstrate your attention to detail and ability to work collaboratively.
Proofread Your Application: Ensure that your CV and cover letter are free from errors. Given the nature of the job, attention to detail is crucial, so take the time to review your application thoroughly before submitting it.
How to prepare for a job interview at Jobster
✨Know Your Regulatory Standards
Familiarise yourself with key regulatory writing standards such as ICH and GCP. Being able to discuss these in detail will show your expertise and understanding of the role.
✨Prepare Examples of Your Work
Have specific examples of regulatory documents you've written or edited ready to discuss. This will demonstrate your experience and ability to produce high-quality work.
✨Showcase Your Attention to Detail
Highlight instances where your attention to detail made a significant impact on a project. This is crucial in regulatory writing, so be prepared to share relevant stories.
✨Ask Insightful Questions
Prepare thoughtful questions about the company's projects and team dynamics. This shows your interest in the role and helps you assess if it's the right fit for you.
