At a Glance
- Tasks: Lead the development of clinical study documents and collaborate with diverse teams.
- Company: Join ICON plc, a world leader in healthcare intelligence and clinical research.
- Benefits: Enjoy competitive salary, health insurance, flexible benefits, and work-life balance.
- Other info: Inclusive culture focused on talent development and career growth.
- Why this job: Make a real impact on innovative treatments while mentoring junior writers.
- Qualifications: Advanced degree in Life Sciences and 3-5 years of medical writing experience required.
The predicted salary is between 55000 - 65000 € per year.
ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development. We are currently seeking a Senior or Principal Medical Writer to join our diverse and dynamic team.
As a Medical Writer at ICON, you will play a pivotal role in leading the development and execution of medical writing strategies for clinical research projects, contributing to the advancement of innovative treatments and therapies.
What you will be doing:
- Leading the preparation, review, and editing of clinical study documents, including clinical study protocols, clinical study reports (CSRs), investigator brochures (IBs), and regulatory submissions, ensuring accuracy, clarity, and compliance with regulatory guidelines and industry standards.
- Collaborating closely with cross‑functional teams, including clinical research, biostatistics, regulatory affairs, and medical affairs, to interpret and analyze clinical trial data, summarise scientific findings, and communicate key insights in written form.
- Participating in the planning and execution of clinical development programs, providing strategic input and scientific expertise to support the design, conduct, and interpretation of clinical studies and research initiatives.
- Contributing to the development of publication plans, abstracts, posters, and manuscripts for submission to peer‑reviewed journals and presentation at scientific conferences, disseminating study results and scientific insights to the broader scientific community.
- Mentoring and coaching junior medical writers, providing guidance on best practices, writing techniques, and scientific principles, and fostering a culture of excellence, collaboration, and continuous learning within the medical writing team.
Your profile:
- Advanced degree in Life Sciences, Pharmacy, Medicine, or related field, with a minimum of 3‑5 years of experience in medical writing within the pharmaceutical, biotechnology, or contract research organization (CRO) industry.
- Proficiency in interpreting and summarising complex clinical trial data, scientific research findings, and statistical analyses, with excellent writing, editing, and proofreading skills, and the ability to communicate scientific concepts to diverse audiences.
- Strong understanding of regulatory requirements (e.g., ICH‑GCP, FDA, EMA) governing the preparation and submission of clinical documents and publications, and experience in interacting with regulatory agencies during the review and approval process.
- Demonstrated ability to work effectively in a fast‑paced, deadline‑driven environment, managing multiple projects simultaneously and prioritising tasks based on project timelines and deliverables.
- Excellent interpersonal and communication skills, with the ability to collaborate effectively with cross‑functional teams, build relationships with key stakeholders, and influence decision‑making processes.
What ICON can offer you:
Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent. In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well‑being and work life balance opportunities for you and your family.
- Various annual leave entitlements
- A range of health insurance offerings to suit you and your family’s needs.
- Competitive retirement planning offerings to maximise savings and plan with confidence for the years ahead.
- Global Employee Assistance Programme, LifeWorks, offering 24‑hour access to a global network of over 80,000 independent specialised professionals who are there to support you and your family’s well‑being.
- Life assurance
- Flexible country‑specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others.
At ICON, inclusion & belonging are fundamental to our culture and values. We’re dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, colour, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.
If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here.
Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless – there’s every chance you’re exactly what we’re looking for here at ICON whether it is for this or other roles.
Senior or Principal Medical Writer in Reading employer: ICON
At ICON plc, we pride ourselves on being a world-leading healthcare intelligence and clinical research organisation that champions innovation and excellence. Our inclusive work culture fosters collaboration and continuous learning, providing ample opportunities for professional growth and development. With competitive benefits tailored to support your well-being and work-life balance, joining our dynamic team as a Senior or Principal Medical Writer means contributing to groundbreaking clinical research while enjoying a fulfilling career in a supportive environment.
StudySmarter Expert Advice🤫
We think this is how you could land Senior or Principal Medical Writer in Reading
✨Tip Number 1
Network like a pro! Reach out to your connections in the medical writing field and let them know you're on the lookout for opportunities. You never know who might have the inside scoop on a role at ICON or can put in a good word for you.
✨Tip Number 2
Prepare for interviews by brushing up on your knowledge of regulatory requirements and clinical trial processes. Be ready to discuss how your experience aligns with ICON's mission and values, and don’t forget to showcase your collaborative spirit!
✨Tip Number 3
Showcase your writing skills! Bring samples of your previous work to the interview, especially those that demonstrate your ability to communicate complex scientific concepts clearly. This will help us see your potential as a Senior or Principal Medical Writer.
✨Tip Number 4
Don’t hesitate to apply through our website! Even if you’re unsure about meeting every requirement, we encourage you to throw your hat in the ring. You might just be the perfect fit for our diverse team at ICON.
We think you need these skills to ace Senior or Principal Medical Writer in Reading
Some tips for your application 🫡
Tailor Your Application:Make sure to customise your CV and cover letter for the Senior or Principal Medical Writer role. Highlight your relevant experience in medical writing and how it aligns with our mission at ICON. We want to see how you can contribute to our innovative projects!
Showcase Your Skills:Don’t just list your qualifications; demonstrate your writing prowess! Include examples of clinical study documents you've worked on, and explain your role in those projects. This will help us see your expertise in action.
Be Clear and Concise:When writing your application, clarity is key. Use straightforward language and avoid jargon where possible. We appreciate well-structured documents that are easy to read, as this reflects the quality we expect in our medical writing.
Apply Through Our Website:We encourage you to apply directly through our careers site. It’s the best way to ensure your application gets into the right hands. Plus, you’ll find more information about the benefits and culture at ICON that make us a great place to work!
How to prepare for a job interview at ICON
✨Know Your Stuff
Make sure you brush up on your knowledge of clinical study documents and regulatory guidelines. Familiarise yourself with ICH-GCP, FDA, and EMA requirements, as well as the types of documents you'll be working on, like CSRs and IBs. This will show that you're not just a great writer but also understand the context of your work.
✨Showcase Your Collaboration Skills
Since the role involves working closely with cross-functional teams, prepare examples of how you've successfully collaborated in the past. Think about specific projects where you worked with clinical research, biostatistics, or regulatory affairs, and be ready to discuss how you contributed to the team's success.
✨Prepare for Technical Questions
Expect some technical questions related to interpreting clinical trial data and summarising scientific findings. Brush up on your statistical knowledge and be ready to explain complex concepts in simple terms. This will demonstrate your ability to communicate effectively with diverse audiences.
✨Mentorship Matters
If you have experience mentoring junior writers, be sure to highlight this during your interview. Discuss your approach to coaching and how you foster a culture of excellence within your team. This shows that you’re not only a skilled writer but also a leader who can help elevate others.
