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- Tasks: Join a dynamic Medical Writing team, crafting essential regulatory documents for innovative biotech projects.
- Company: Barrington James represents a rapidly growing biotech firm in Europe, backed by top industry investors.
- Benefits: Enjoy the flexibility of freelance work while contributing to groundbreaking studies in the biotech field.
- Why this job: Be part of an ambitious company making waves in the market with cutting-edge research and development.
- Qualifications: Must have over 5 years of regulatory writing experience and a strong background in bio/pharma.
- Other info: Apply quickly as this popular opportunity may close sooner than expected!
The predicted salary is between 48000 - 72000 £ per year.
Barrington James are exited to post a fantastic opportunity for one of our close clients. This company is a small Biotech in Europe that has exploded in size in recent years. They are backed by some serious investors the industry and are looking for future support within their Medical Writing team. This opportunity is prefect for someone who is ambitious, independent and wants to play a key role in working on the most innovative projects.
Requirements:
- Over years 5 years working on a range of Regulatory documents
- Over 10 years in Bio/Pharma companies
- Experience in early stage clinical trials working on CSR\’s and CSP\’s
- Experience on a range of CTD modules including M2.5, M2.7 2.7.3 & 2.7.4
- Experience on protocols, IBs & briefing books would be ideal
This truly is an exiting opportunity for someone to join an ambitious company who are continuing to impress the market with their ground-breaking studies.
The opportunity has understandably been incredibly popular. We encourage all interested candidates to apply immediately as it is likely that recruitment will close prematurely.
By clicking \”apply\” you will be sending your CV to Charlie Denton at Barrington James. Charlie is a specialist Medical Writer recruiter and will discuss the opportunity in detail with you, facilitate your application and will manage the process acting as a link between the company and yourself.
Please call +44 12 93 77 66 44 if you have any questions, alternatively you can reach Charlie on
Freelance regulatory writer employer: Barrington James
Contact Detail:
Barrington James Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Freelance regulatory writer
✨Tip Number 1
Network with professionals in the biotech and regulatory writing fields. Attend industry conferences or webinars where you can meet people who work at companies similar to our client. This can help you get insider information about the company culture and potentially a referral.
✨Tip Number 2
Familiarise yourself with the latest trends and regulations in the biotech sector. Being knowledgeable about current developments will not only boost your confidence but also impress recruiters during any discussions.
✨Tip Number 3
Prepare to discuss specific projects you've worked on that align with the requirements listed in the job description. Highlight your experience with regulatory documents and early-stage clinical trials to demonstrate your suitability for the role.
✨Tip Number 4
Reach out to Charlie Denton directly if you have questions about the role. Engaging with the recruiter shows your enthusiasm and can help you stand out from other candidates. Plus, it gives you a chance to clarify any details before applying.
We think you need these skills to ace Freelance regulatory writer
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights your relevant experience in regulatory writing, particularly focusing on your 5+ years of work with regulatory documents and your background in Bio/Pharma companies. Emphasise any specific projects related to early-stage clinical trials.
Craft a Compelling Cover Letter: Write a cover letter that showcases your ambition and independence. Mention your familiarity with CTD modules and your experience with CSR's and CSP's. This is your chance to express why you are excited about the opportunity and how you can contribute to the Medical Writing team.
Highlight Relevant Skills: In your application, clearly outline your skills related to protocols, IBs, and briefing books. Use specific examples from your past work to demonstrate your expertise and how it aligns with the company's needs.
Follow Up: After submitting your application through our website, consider following up with Charlie Denton at Barrington James. A polite email or call can show your enthusiasm for the position and keep you on their radar during the selection process.
How to prepare for a job interview at Barrington James
✨Showcase Your Regulatory Expertise
Make sure to highlight your extensive experience with regulatory documents during the interview. Be prepared to discuss specific examples of CTD modules you've worked on, especially M2.5, M2.7, 2.7.3, and 2.7.4, as well as your involvement in early-stage clinical trials.
✨Demonstrate Your Independence
Since the company is looking for someone ambitious and independent, be ready to share instances where you took initiative or led projects. This will show that you can thrive in a fast-paced environment and contribute significantly to their innovative projects.
✨Prepare for Technical Questions
Expect technical questions related to medical writing and regulatory processes. Brush up on your knowledge of protocols, IBs, and briefing books, as these are ideal experiences they are looking for. Being well-prepared will help you stand out.
✨Express Enthusiasm for the Company
Research the company and its recent achievements in the biotech field. Showing genuine enthusiasm for their groundbreaking studies and expressing how you can contribute to their success will leave a positive impression on the interviewers.
