Senior Medical Writer

🔥 8 minutes ago

🌐 United Kingdom, Spain, +8 more countries – Remote

🇬🇧 United Kingdom – Remote 🇪🇸 Spain – Remote 🇧🇬 Bulgaria – Remote 🇷🇴 Romania – Remote 🇩🇪 Germany – Remote 🇵🇹 Portugal – Remote 🇬🇷 Greece – Remote 🇵🇱 Poland – Remote 🇫🇷 France – Remote 🇮🇹 Italy – Remote

⏰ Full Time

🟠 Senior

🏥📝 Medical Writer

👻 Ghost score 10%

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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

• Provide scientific and medical/clinical writing support as part of a team dedicated to late-phase projects, servicing an assigned client • Work closely with the ICON team and other members of the client account team to ensure timely delivery of high-quality and scientifically/medically accurate assigned projects • Work with Peri- and Post-Approval Safety studies and RWE studies • Write and review study documents such as Protocol, Synopsis, Informed Consent, Data Collection Documents and Study Report • Develop scientific communications such as abstracts, posters, and manuscripts • Perform quality control for medical writing deliverables • Interpret statistical results and solicit statistician input for study reports, abstracts, manuscripts, and other documents • Participate in improvement of the quality assurance system • Participate in bid-defence presentations representing medical writing activities

🎯 Requirements

• Advanced degree in a scientific discipline, PharmD • 4+ years of professional experience in Medical Writing at a pharmaceutical, biotechnology, CRO or other health care setting • Proven knowledge of ICH/GCP and GPP guidelines or other meaningful guidelines or industry standard • Outstanding written and verbal interpersonal skills • Good computer literacy • Ability to work effectively and cooperatively with cross-functional teams • 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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