Clinical Editor

Job not on LinkedIn

🔥 0 minutes ago

🌐 United Kingdom, France, +3 more countries – Remote

🇬🇧 United Kingdom – Remote 🇫🇷 France – Remote 🇩🇪 Germany – Remote 🇨🇭 Switzerland – Remote 🇪🇸 Spain – Remote

⏰ Full Time

🟡 Mid-level

🟠 Senior

✏️ Editor

👻 Ghost score 10%

What it means: the chance that no one is really hiring for this job.How to read it: 60% or higher means we think this is a ghost. Lower scores are less of a worry.How we score it: age, reposts, open roles vs team size, how fast jobs close, and whether pay is listed.Fine print: an estimate from public data, not a judgment of the company. Real jobs can score high, so treat it as a hint, not a fact.

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ICON plc

WebsiteLinkedInAll Job Openings

10,000+ employees

Founded 1990

💼 Consulting

🏥 Healthcare

📦 Logistics

Consulting • Healthcare • Logistics

ICON plc is a global provider of clinical, consulting, and commercial services across various sectors in the healthcare and pharmaceutical industries. They offer a wide range of clinical solutions, including decentralised clinical trials, cardiac safety solutions, early clinical laboratories, and medical imaging. ICON also provides technology solutions that support drug development from early phases to post-marketing. Their therapeutic expertise spans cardiovascular, oncology, internal medicine, and more, with a strong focus on transformative therapies like cell and gene therapies and biosimilars. ICON is recognized as a leading Contract Research Organisation (CRO), regularly providing thought leadership and contributing to industry publications and events. Their services are tailored to optimize clinical trials, offer regulatory intelligence, and deliver real-world evidence through robust data analysis and patient-centric solutions.

📋 Description

• Perform quality reviews and edit clinical documents, regulatory submissions, and other related documents • Perform detailed data accuracy reviews and fact-check statements in clinical and regulatory documents, tables, literature summaries, and other internal documents • Substantively edit and proofread documents to correct and streamline grammar, spelling, style, and format • Verify document content is consistent with internal, client, and related authority guidelines • Format, style, and troubleshoot functionality and presentation of documents and templates • Communicate with medical writers and other team members to ensure document accuracy • Ensure inspection-readiness of medical writing activities

🎯 Requirements

• Bachelor's degree in a relevant scientific discipline • At least 3 years of experience in medical editing or scientific writing, preferably within a clinical research or pharmaceutical environment • Strong knowledge of medical terminology and an understanding of clinical research processes and regulations • Excellent language skills (reading, writing, editing, team communication) • Ability to interpret clinical data and literature • Knowledge of AMA Manual of Style, other style guides, and any guidelines related to assigned projects • Expertise in Microsoft Word, including advanced formatting, styles, cross-referencing, bookmarks, and other related skills • Fluent in English • Basic understanding of Acrobat/PDF software • Legal right to work in the country where the role is based

🏖️ Benefits

• Competitive base salary and performance related incentives • Health and wellbeing programmes including medical, dental, and vision coverage where applicable • Retirement and pension plans • Life assurance and disability coverage • Employee assistance programmes and wellbeing resources • Learning and development opportunities through structured training and career pathways

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