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- Tasks: Join a dynamic Medical Writing team, crafting essential regulatory documents for innovative biotech projects.
- Company: A rapidly growing European biotech firm backed by top industry investors.
- Benefits: Enjoy flexible freelance work with the chance to impact groundbreaking studies.
- Why this job: Be part of an ambitious company making waves in the biotech sector with exciting projects.
- Qualifications: 5+ years in regulatory writing and 10+ years in bio/pharma, with experience in clinical trials.
- Other info: Apply quickly as this popular role may close soon; connect with specialist recruiter Charlie Denton.
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 potential colleagues and learn about the latest trends. This can help you get your foot in the door and may lead to referrals.
✨Tip Number 2
Showcase your expertise in regulatory documents by engaging in relevant online forums or groups. Share your insights and experiences, which can help establish your credibility and attract attention from recruiters looking for someone with your background.
✨Tip Number 3
Consider reaching out directly to the hiring manager or recruiter, Charlie Denton, via LinkedIn or email. Express your enthusiasm for the role and briefly highlight your relevant experience. A personal touch can make a significant difference in a competitive job market.
✨Tip Number 4
Stay updated on the latest developments in regulatory writing and biotech innovations. Being knowledgeable about current trends will not only prepare you for interviews but also demonstrate your passion for the field when discussing your experience.
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 CTD modules you've worked on.
Craft a Compelling Cover Letter: Write a cover letter that showcases your ambition and independence. Mention your experience with early-stage clinical trials and how it aligns with the innovative projects at the company. Be sure to express your enthusiasm for the opportunity.
Highlight Key Skills: In your application, clearly outline your skills related to protocols, IBs, and briefing books. This will demonstrate your comprehensive understanding of the regulatory landscape and make you stand out as a candidate.
Follow Up: After submitting your application through our website, consider following up with Charlie Denton. A brief email expressing your continued interest can help keep your application top of mind.
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, particularly 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 dynamic environment and contribute significantly to their innovative projects.
✨Prepare for Technical Questions
Expect technical questions related to your experience with Clinical Study Reports (CSRs) and Clinical Study Protocols (CSPs). Brush up on the specifics of these documents and be ready to explain your role in their development.
✨Express Enthusiasm for Innovation
The company prides itself on being at the forefront of groundbreaking studies. Convey your passion for innovation in the biotech field and how you can contribute to their mission. This will resonate well with the interviewers and demonstrate your alignment with their goals.
