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For Companies At a Glance
- Tasks: Lead exciting projects by writing and reviewing crucial medical documents.
- Company: Join a leading CRO in Manchester, known for its innovative approach.
- Benefits: Enjoy flexible working options and opportunities for professional growth.
- Why this job: Make a real impact in healthcare while mentoring the next generation of writers.
- Qualifications: Extensive experience in medical writing and regulatory roles is essential.
- Other info: Work across various therapy areas and manage multiple projects simultaneously.
The predicted salary is between 36000 - 60000 £ per year.
The Role
Working on a number of exciting projects and with an exciting pipeline, the Principal Medical Writer (Regulatory) will be responsible for:
- Writing, editing, and reviewing documents such as Clinical Study Reports, Protocols, Informed Consent forms, Safety Aggregate Reports (DSUR/PBRER), Safety Narratives, Clinical summaries / CTD sections, and Clinical Overviews.
- Managing multiple projects concurrently, taking the lead on projects.
- Mentoring junior team members.
- Reviewing all documentation to a high standard.
- Working across multiple therapy areas.
- Meeting internal and external deliverables within set timelines.
You
To apply for this role as Principal Medical Writer (Regulatory / Clinical), our client is looking for someone with:
- Extensive experience in Medical Writing / Regulatory Writing roles.
- Experience within a CRO or pharmaceutical setting.
- Proven ability to write, edit, and review documents such as Clinical Study Reports, Protocols, Informed Consent forms, Safety Reports, and Clinical Summaries.
- The ability to work in a fast-paced environment, meeting tight deadlines.
Principle Medical Writer – Leading CRO employer: Carrot Recruitment
Contact Detail:
Carrot Recruitment Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Principle Medical Writer – Leading CRO
✨Tip Number 1
Network with professionals in the medical writing field, especially those who work in CROs or pharmaceutical companies. Attend industry conferences or webinars to connect with potential colleagues and learn about the latest trends in regulatory writing.
✨Tip Number 2
Familiarise yourself with the specific types of documents mentioned in the job description, such as Clinical Study Reports and Safety Aggregate Reports. Consider creating a portfolio that showcases your experience with these documents to demonstrate your expertise during interviews.
✨Tip Number 3
Prepare for the interview by brushing up on your project management skills. Be ready to discuss how you manage multiple projects and meet tight deadlines, as this is crucial for the Principal Medical Writer role.
✨Tip Number 4
Research the company culture and values of the CRO you're applying to. Tailor your conversation during the interview to reflect how your personal values align with theirs, which can help you stand out as a candidate.
We think you need these skills to ace Principle Medical Writer – Leading CRO
Some tips for your application 🫡
Understand the Role: Before applying, make sure you fully understand the responsibilities of a Principal Medical Writer. Familiarise yourself with the types of documents you'll be expected to write and review, such as Clinical Study Reports and Protocols.
Tailor Your CV: Highlight your relevant experience in Medical Writing and Regulatory Writing. Be specific about your previous roles in CRO or pharmaceutical settings, and include examples of documents you've worked on that align with the job description.
Craft a Compelling Cover Letter: Use your cover letter to showcase your passion for medical writing and your ability to manage multiple projects. Mention any mentoring experience you have, as this is a key aspect of the role.
Proofread Your Application: Ensure that your CV and cover letter are free from errors. Given the nature of the role, attention to detail is crucial. Consider asking a colleague or friend to review your application before submission.
How to prepare for a job interview at Carrot Recruitment
✨Showcase Your Writing Skills
As a Principal Medical Writer, your writing ability is crucial. Bring samples of your previous work to the interview, especially documents like Clinical Study Reports or Protocols. Be prepared to discuss your writing process and how you ensure accuracy and clarity in your documents.
✨Demonstrate Project Management Experience
Since the role involves managing multiple projects, be ready to share examples of how you've successfully juggled various tasks in the past. Highlight your organisational skills and any tools or methods you use to keep projects on track.
✨Emphasise Mentoring Skills
The position requires mentoring junior team members, so think about times when you've guided others. Discuss your approach to mentoring and how you help less experienced colleagues develop their skills in medical writing.
✨Prepare for Technical Questions
Expect questions related to regulatory writing and the specific types of documents you'll be handling. Brush up on relevant guidelines and best practices in medical writing to demonstrate your expertise and confidence during the interview.
