Medical Content Developer
2 days ago
Clinical research is at the heart of what we do at ICON. Our team of experts is dedicated to advancing innovative treatments and therapies through the development and preparation of clinical trial documents, regulatory submissions, and scientific publications.
We are currently seeking a skilled Medical Writer II to join our team. In this role, you will play a key part in preparing, writing, and editing clinical study reports (CSRs), clinical protocols, investigator brochures (IBs), patient narratives, and other regulatory documents in compliance with internal standards and regulatory guidelines.
The ideal candidate will have a strong background in medical writing, with a minimum of 3 years of experience in the pharmaceutical, biotechnology, or contract research organization (CRO) industry. You will need to have proficiency in scientific and medical terminology, excellent written and verbal communication skills, attention to detail, and the ability to convey complex information in a clear and concise manner.
You will also be responsible for conducting literature reviews, data analysis, and interpretation of clinical trial results to support the development of scientific manuscripts, abstracts, posters, and presentations for publication in peer-reviewed journals and scientific conferences. A strong understanding of regulatory requirements, industry guidelines, and publication standards governing the preparation and submission of clinical trial documents and scientific manuscripts is also essential.
As a valued member of our team, you can expect a competitive salary, plus a range of benefits designed to support your well-being and work-life balance. These include various annual leave entitlements, health insurance options, competitive retirement planning offerings, and access to our Global Employee Assistance Programme, LifeWorks.
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