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- Tasks: Write and edit clinical documents, ensuring clarity and accuracy in scientific information.
- Company: Join a leading company dedicated to high-quality medical writing and regulatory compliance.
- Benefits: Enjoy competitive pay, flexible hours, and opportunities for professional growth.
- Other info: Collaborative environment with potential for career advancement and minimal travel.
- Why this job: Make a difference in healthcare by communicating vital scientific information effectively.
- Qualifications: Strong writing skills and a passion for science are essential.
The predicted salary is between 40000 - 50000 £ per year.
Medical writer on clinical study or regulatory project teams. Writes, edits, and coordinates content for clinical/regulatory documents to ensure high-quality completion of all assigned writing projects.
Job Responsibilities
- Compiles, writes, edits, and coordinates medical writing deliverables that present scientific information clearly and accurately, and works as a medical writer within and across departments with moderate supervision.
- Completes a variety of documents that may include clinical study protocols and protocol amendments; clinical study reports; patient narratives; and investigator brochures.
- Adheres to established regulatory standards, including ICH E3 guidelines, company standard operating procedures, client standards, company and/or client-approved templates, authorship requirements, and style and formatting guides, when completing medical writing projects, on time and on budget.
- Coordinates quality and editorial reviews. Ensures source documentation is managed appropriately. Leads document reviews, reviews documents as needed, and resolves comments from client.
- Reviews statistical analysis plans and table/figure/listing specifications for appropriate content and for grammar, format, and consistency.
- Interacts and builds good working relationships with clients, department head, and peers, as necessary, to produce writing deliverables.
- Performs online clinical literature searches and complies with copyright requirements.
- Identifies and proposes solutions to resolve document issues, escalating as appropriate.
- Continues professional development to grow awareness of industry standards and best practices to improve ability to meet client expectations.
- Aware of budget specifications for assigned projects, working within the budgeted hours and communicating status and changes to medical writing leadership.
- Completes required administrative tasks within the specified timeframes. Performs other work-related duties as assigned.
- Minimal travel may be required (less than 25%).
Medical Writer in London employer: Syneos Health, Inc.
Contact Detail:
Syneos Health, Inc. Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Medical Writer in London
✨Tip Number 1
Network like a pro! Reach out to professionals in the medical writing field on LinkedIn or at industry events. Building connections can lead to job opportunities that aren’t even advertised yet.
✨Tip Number 2
Show off your skills! Create a portfolio showcasing your best writing samples, especially those related to clinical studies or regulatory documents. This will give potential employers a taste of what you can do.
✨Tip Number 3
Prepare for interviews by brushing up on ICH E3 guidelines and other relevant regulations. Being knowledgeable about industry standards will impress interviewers and show you’re serious about the role.
✨Tip Number 4
Don’t forget to apply through our website! We’ve got loads of opportunities waiting for talented medical writers like you. Plus, it’s the best way to ensure your application gets seen by the right people.
We think you need these skills to ace Medical Writer in London
Some tips for your application 🫡
Tailor Your Application: Make sure to customise your CV and cover letter for the Medical Writer role. Highlight your experience with clinical documents and any familiarity with regulatory standards like ICH E3. We want to see how your skills match what we're looking for!
Showcase Your Writing Skills: Since this is a writing position, include samples of your previous work if possible. Whether it's clinical study protocols or reports, we love seeing how you present scientific information clearly and accurately.
Be Detail-Oriented: Pay attention to grammar, formatting, and consistency in your application. This role requires a keen eye for detail, so make sure your application reflects that. We appreciate candidates who can spot the little things!
Apply Through Our Website: We encourage you to submit your application through our website. It’s the best way for us to receive your details and ensures you’re considered for the role. Plus, it’s super easy to do!
How to prepare for a job interview at Syneos Health, Inc.
✨Know Your Documents
Familiarise yourself with the types of documents you'll be working on, like clinical study protocols and reports. Being able to discuss these confidently will show your understanding of the role and impress the interviewers.
✨Brush Up on Regulatory Standards
Make sure you understand ICH E3 guidelines and other relevant regulatory standards. This knowledge is crucial for a Medical Writer, and demonstrating it in your interview will highlight your preparedness and commitment to quality.
✨Showcase Your Collaboration Skills
Since the role involves working across departments, be ready to share examples of how you've successfully collaborated in the past. Highlighting your ability to build relationships will resonate well with the interviewers.
✨Prepare for Quality Control Questions
Expect questions about how you handle document reviews and quality checks. Be prepared to discuss your process for ensuring accuracy and consistency in your writing, as this is key to the role.