Medical and Scientific Writer II

Medical and Scientific Writer II - Dublin - Hybrid

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 Medical and Scientific Writer II to join our diverse and dynamic team. As a Medical and Scientific Writer II at ICON, you will play a pivotal role in developing and preparing clinical trial documents, regulatory submissions, and scientific publications, contributing to the advancement of innovative treatments and therapies.

What you will be doing

1. Collaborate with cross-functional teams to prepare, write, and edit clinical study reports (CSRs), clinical protocols, investigator brochures (IBs), patient narratives, and other regulatory documents in compliance with internal standards and regulatory guidelines.
2. Conduct literature reviews, data analysis, and interpretation of clinical trial results to support scientific manuscripts, abstracts, posters, and presentations for publication in peer-reviewed journals and scientific conferences.
3. Assist in reviewing and validating clinical data, ensuring accuracy, completeness, and consistency with study protocols, SOPs, and regulatory requirements.
4. Participate in project meetings, teleconferences, and client interactions to discuss project objectives, timelines, and deliverables, providing input and feedback on document content, format, and presentation.
5. Stay updated on emerging trends, scientific developments, and regulatory updates in relevant therapeutic areas, applying knowledge of medical writing principles to support clinical research projects.

Your profile

1. Bachelor's degree in Life Sciences, Pharmacy, Medicine, or related field, with at least 3 years of medical writing experience within the pharmaceutical, biotech, or CRO industry.
2. Proficiency in scientific and medical terminology, with excellent written and verbal communication skills, attention to detail, and the ability to convey complex information clearly and concisely.
3. Strong analytical and critical thinking skills to review and interpret clinical data, identify key findings, and communicate results effectively to stakeholders.
4. Familiarity with regulatory requirements, industry guidelines, and publication standards for clinical trial documents and scientific manuscripts.
5. Proficiency in Microsoft Office (Word, Excel, PowerPoint) and familiarity with document management, reference software, and statistical analysis tools is preferred.

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What ICON can offer you:

Our success depends on the quality of our people. We've prioritized building a diverse culture that rewards high performance and nurtures talent.

In addition to a competitive salary, ICON offers various benefits focused on well-being and work-life balance, including:

- Annual leave entitlements
- Health insurance options for you and your family
- Retirement planning options
- Global Employee Assistance Programme, LifeWorks, providing 24/7 support from a network of professionals
- Life assurance
- Flexible country-specific benefits like childcare vouchers, bike schemes, gym discounts, travel passes, and health assessments

Visit our careers site to learn more about ICON's benefits.

At ICON, inclusion & belonging are core to our culture. We are committed to providing an accessible, discrimination-free workplace. If you need accommodations during the application process due to a medical condition or disability, please let us know or submit a request here.

Interested but unsure if you meet all requirements? We encourage you to apply—your skills might be exactly what we're looking for.

If you're a current ICON employee, please apply here.

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