Senior Medical Data Reviewer

🔥 34 minutes ago

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

🇬🇧 United Kingdom – Remote 🇵🇱 Poland – Remote 🇸🇰 Slovakia – Remote 🇮🇪 Ireland – Remote 🇿🇦 South Africa – Remote

⏰ Full Time

🟠 Senior

👻 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 expert medical oversight of clinical trial data, ensuring accuracy, consistency, and patient safety • Take ownership of clinical research deliverables and apply expertise to complex challenges • Perform advanced medical review of clinical data listings, patient profiles, and safety datasets • Identify trends, potential safety signals, and data quality issues and collaborate with study teams to drive resolution • Contribute to or lead development of medical review plans, guidelines, and tools for complex studies or programmes • Provide medical input into database lock readiness, interim analyses, and regulatory submission preparation • Collaborate with pharmacovigilance, biostatistics, and data management on integrated safety and efficacy evaluations • Mentor junior medical data reviewers and support continuous improvement of review methodologies

🎯 Requirements

• Medical degree or advanced clinical qualification (e.g., MD, MBBS, PharmD) with relevant clinical experience • Extensive experience in clinical research, medical monitoring, pharmacovigilance, or related roles within CRO, pharma, or biotech • Deep understanding of clinical trial design, GCP, safety reporting, and medical terminology • Excellent analytical and critical-thinking skills, with a high level of attention to detail in data review • Strong communication and collaboration skills, with experience working in cross-functional, global teams • Ability to manage multiple studies and priorities while maintaining high quality and timelines • 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