Statistical Programmer I

🔥 50 minutes ago

🌐 Romania, Kenya, +4 more countries – Remote

🇷🇴 Romania – Remote 🇰🇪 Kenya – Remote 🇵🇱 Poland – Remote 🇭🇺 Hungary – Remote 🇿🇦 South Africa – Remote 🇧🇬 Bulgaria – Remote

⏰ Full Time

🟢 Junior

🖥 Software Engineer

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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

• Develop, validate, and maintain complex statistical programs, primarily in R, for clinical trial data analysis and reporting • Take ownership of one or more studies • Work alongside Principal Programmers and act as a key contact for a leading FSP sponsor • Partner with biostatisticians and cross-functional colleagues to translate study requirements into statistical outputs • Prepare and review statistical analysis plans, programming specifications, and derived datasets • Safeguard data integrity and adhere to ICH/GCP standards • Mentor junior programmers • Contribute to knowledge-sharing and continuous improvement

🎯 Requirements

• A degree in statistics, mathematics, computer science, or a related field • 1+ year of experience as a statistical programmer within clinical research • Hands-on experience in R programming, ideally 1+ years in a clinical trials setting • A sharp analytical mindset, attention to detail, and confidence working independently • Ability to explain complex statistical concepts clearly and collaborate with technical and non-technical stakeholders • 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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