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For Companies At a Glance
- Tasks: Write and prepare Clinical Study Reports for Phase 1, ensuring compliance with regulatory guidelines.
- Company: Join a leading client in the clinical research field with a focus on innovation.
- Benefits: Flexible working arrangements and opportunities for professional growth.
- Why this job: Make a real impact in clinical research while honing your scientific writing skills.
- Qualifications: Strong report writing experience and attention to detail are essential.
- Other info: Ideal for freelancers or those looking to break into the clinical sector.
The predicted salary is between 36000 - 60000 £ per year.
We have an amazing client looking for a CSR Writer to support a full Clinical Study Report writing for Phase 1, development and preparation of regulatory Modules (2.7.1/2.7.2). They are looking for strong scientific writing skills, a key attention to detail and inspection‐ready deliverables.
Key Responsibilities
- All deliverables are inspection ready and compliant with regulatory guidelines
- Maintain planning for writing and QC deliverables
- Highlight any process improvements to enhance collaboration between CPP and document Service Teams
- Excel in shell creation and timeline management
- Create QC reports
- Interpret clinical and statistical outputs
Skills
- Strong experience in report writing and QC procedures
- Formal communication skills
- Excellent knowledge of formatting on Word
An Ideal Candidate
- Understanding of PK/PD analysis tools
- Working understanding of Phoenix WinNonlin
If you are a contract freelancer in CSR or looking to move into this sector please apply below and I would love to hear from you to discuss the vacancy further.
Clinical Study Report – Clinical Pharmacology in London employer: Barrington James Limited
Contact Detail:
Barrington James Limited Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Clinical Study Report – Clinical Pharmacology in London
✨Tip Number 1
Network like a pro! Reach out to professionals in the clinical pharmacology field on LinkedIn or at industry events. We can’t stress enough how valuable personal connections can be in landing that dream job.
✨Tip Number 2
Showcase your skills! Create a portfolio of your best CSR writing samples and any relevant projects. This will give potential employers a taste of what you can bring to the table, and we all know first impressions count!
✨Tip Number 3
Prepare for interviews by brushing up on your knowledge of PK/PD analysis tools and regulatory guidelines. We recommend practising common interview questions related to scientific writing and QC procedures to boost your confidence.
✨Tip Number 4
Don’t forget to apply through our website! It’s the easiest way to get your application noticed. Plus, we’re always on the lookout for talented individuals who are ready to make an impact in the clinical study report space.
We think you need these skills to ace Clinical Study Report – Clinical Pharmacology in London
Some tips for your application 🫡
Show Off Your Writing Skills: Since strong scientific writing is key for this role, make sure your application showcases your best writing. Use clear, concise language and demonstrate your ability to convey complex information effectively.
Attention to Detail is Key: We can't stress this enough! Double-check your application for any typos or formatting issues. Remember, if you want to impress us with your attention to detail, it starts right here in your application.
Tailor Your Application: Make sure to customise your CV and cover letter to highlight relevant experience, especially in CSR writing and regulatory guidelines. We want to see how your background aligns with what we're looking for!
Apply Through Our Website: To make the process smoother for both of us, please apply through our website. It helps us keep track of applications and ensures you get the best chance at standing out!
How to prepare for a job interview at Barrington James Limited
✨Master the Basics of CSR Writing
Before your interview, brush up on the fundamentals of Clinical Study Report writing. Familiarise yourself with the structure and key components of a CSR, especially for Phase 1 studies. This will show that you understand the role and can hit the ground running.
✨Showcase Your Attention to Detail
Prepare examples from your past work where your attention to detail made a significant impact. Whether it was catching errors in a report or ensuring compliance with regulatory guidelines, be ready to discuss how this skill is crucial in producing inspection-ready deliverables.
✨Familiarise Yourself with Regulatory Modules
Make sure you know the ins and outs of regulatory Modules 2.7.1 and 2.7.2. Being able to discuss these modules confidently will demonstrate your preparedness and understanding of the regulatory landscape, which is vital for the role.
✨Prepare for Technical Questions
Expect questions about PK/PD analysis tools and Phoenix WinNonlin. Brush up on your technical knowledge and be ready to explain how you've used these tools in your previous roles. This will help you stand out as a candidate who is not only skilled but also technically savvy.
