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- Tasks: Write and coordinate clinical trial documents for innovative pharmaceutical projects.
- Company: Join ICON, a leader in bringing life-improving drugs to market with a culture of innovation.
- Benefits: Enjoy remote work flexibility and the chance to impact global health.
- Why this job: Be part of a dynamic team dedicated to improving lives through groundbreaking research.
- Qualifications: Bachelor’s Degree and 2-3 years of experience in regulatory writing required.
- Other info: This role is exclusively for candidates based in Ireland.
The predicted salary is between 42000 - 84000 £ per year.
As a Senior Medical Writer you will be dedicated to one of our global pharmaceutical clients; a client with which ICON shares a culture of innovation, flexibility and a common vision of bringing life-improving drugs to market. We are also reviewing freelance regulatory medical writers based in Ireland. Please note, this role is open for Ireland location only.
The role involves working on clinical trial documents for Phase 1 and Phase 2 studies.
Writing scope:- Study protocols and protocol amendments
- Initial Investigator's Brochure (IB) and IB updates
- Clinical study reports
- Plan, write, review, and coordinate the development of regulatory clinical trial documents.
- Ensure and coordinate quality checks for accuracy, collate reviewer’s comments, adjust content of documents as required based on internal/external input, and prepare final versions.
- Ensure final documents and supporting quality check documentation (with all signatures where appropriate) are placed in the appropriate document management system.
- Bachelor’s Degree
- 2-3 years of prior experience writing regulatory or clinical trial documents - Protocols/Protocol amendments/IBs
- Demonstrated mastery of written and verbal English
- Demonstrated project management and time management skills
- High-level end-user computer skills (e.g., word processing, tables, and graphics)
- Ability to work well across cultures and time zones
Senior Medical Writer - Ireland home based employer: ICON
Contact Detail:
ICON Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Senior Medical Writer - Ireland home based
✨Tip Number 1
Familiarise yourself with the specific regulatory requirements and guidelines for clinical trial documents in Ireland. Understanding the nuances of local regulations will not only enhance your writing but also demonstrate your commitment to the role.
✨Tip Number 2
Network with professionals in the pharmaceutical industry, especially those who have experience in medical writing. Engaging with others can provide insights into the role and may even lead to referrals or recommendations.
✨Tip Number 3
Showcase your project management skills by discussing any relevant experiences where you successfully coordinated multiple tasks or projects. This is crucial for a Senior Medical Writer, as you'll need to manage timelines and collaborate with various stakeholders.
✨Tip Number 4
Prepare to discuss your experience with clinical trial documents during interviews. Be ready to provide examples of protocols, amendments, or reports you've worked on, highlighting your attention to detail and ability to incorporate feedback effectively.
We think you need these skills to ace Senior Medical Writer - Ireland home based
Some tips for your application 🫡
Understand the Role: Read the job description thoroughly to understand the specific requirements and responsibilities of the Senior Medical Writer position. Tailor your application to highlight relevant experience in writing clinical trial documents.
Highlight Relevant Experience: In your CV and cover letter, emphasise your 2-3 years of experience in writing regulatory or clinical trial documents. Provide specific examples of study protocols, amendments, or Investigator's Brochures you have worked on.
Showcase Language Proficiency: Since mastery of written and verbal English is crucial, ensure your application is free from grammatical errors. Use clear and concise language to demonstrate your communication skills.
Demonstrate Project Management Skills: Include examples in your application that showcase your project management and time management abilities. Mention any tools or methods you use to coordinate document development and quality checks.
How to prepare for a job interview at ICON
✨Showcase Your Writing Skills
As a Senior Medical Writer, your writing ability is crucial. Bring samples of your previous work, especially clinical trial documents, to demonstrate your expertise and style. Be prepared to discuss your writing process and how you ensure accuracy and clarity in your documents.
✨Understand the Regulatory Landscape
Familiarise yourself with the regulatory requirements for clinical trial documents in Ireland. During the interview, highlight your knowledge of these regulations and how you've applied them in your previous roles. This will show that you are well-prepared and understand the importance of compliance.
✨Demonstrate Project Management Skills
Since the role involves coordinating the development of documents, be ready to discuss your project management experience. Share examples of how you've managed timelines, collaborated with teams, and handled feedback from multiple stakeholders to deliver high-quality documents on time.
✨Cultural Awareness and Flexibility
Given that you'll be working with a global client, it's essential to demonstrate your ability to work across cultures and time zones. Discuss any previous experiences where you've successfully collaborated with international teams, showcasing your adaptability and communication skills.
