As a Senior Medical Writer, you will join the world’s largest & most comprehensive clinical research organization, powered by healthcare intelligence.

What will you be doing?

Research, write, and edit clinical and regulatory documents by applying your expertise in clinical drug development. Your responsibilities include producing clear and concise documents such as study reports, protocols, investigator brochures, and other scientific materials. You should demonstrate excellent written and oral communication skills and be proficient with medical writing tools and software (e.g., PleaseReview, Documentum).

What do you need to have?

• Experience in writing and reviewing clinical study reports, protocols, and regulatory documents.
• Contributing to clinical protocol development, especially for first-in-human oncology studies.
• Technical expertise in medical writing tools and software.
• Ability to produce clear scientific documents and interpret clinical data effectively.
• Knowledge of current guidelines and submission requirements.
• Strong interpersonal and communication skills.
• Proficiency in MS Word, Excel, PowerPoint, and Outlook.
• Ability to manage multiple projects efficiently.

Location: UK or Europe remote

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What ICON can offer you:

We prioritize building a diverse culture that rewards high performance and nurtures talent. ICON offers a competitive salary and a range of benefits focused on well-being and work-life balance, including various leave entitlements, health insurance, retirement plans, and more.

Visit our careers website to learn more about working at ICON: https://careers.iconplc.com/benefits

At ICON, inclusion & belonging are fundamental. We are committed to an inclusive environment and provide accommodations for applicants with disabilities. For accommodations, please visit: https://careers.iconplc.com/reasonable-accommodations

We encourage you to apply even if you don’t meet all the requirements; you might be the perfect fit for this or other roles at ICON.