Statistical Programmer II

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🌐 Poland, Spain, +7 more countries – Remote

🇵🇱 Poland – Remote 🇪🇸 Spain – Remote 🇭🇺 Hungary – Remote 🇬🇧 United Kingdom – Remote 🇧🇬 Bulgaria – Remote 🇷🇴 Romania – Remote 🇰🇪 Kenya – Remote 🇹🇷 Turkey – Remote 🇿🇦 South Africa – Remote

⏰ Full Time

🟡 Mid-level

🟠 Senior

🖥 Software Engineer

👻 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

• Develop, validate and maintain statistical programs to support clinical trial analysis and reporting • Create and review analysis datasets and statistical outputs, including tables, listings and figures • Work with programming languages and industry standards relevant to the client and programme, including R, SDTM and ADaM • Collaborate with biostatisticians and cross-functional clinical teams to deliver high-quality statistical outputs • Perform quality control and validation to ensure accuracy, consistency and data integrity • Contribute to programming strategy, process improvements, automation and standardisation • Take greater ownership of studies and programming activities as experience progresses • Provide technical leadership and support other programmers

🎯 Requirements

• Experience in statistical programming within clinical research, pharmaceutical or biotechnology environments • Strong programming skills relevant to clinical trials • Experience with R and/or CDISC standards such as SDTM and ADaM, depending on your area of expertise • Knowledge of clinical trial data, statistical analysis and reporting • Strong analytical and problem-solving skills with excellent attention to detail • Ability to collaborate effectively with biostatisticians and cross-functional teams • For more experienced programmers, experience taking ownership of studies, providing technical guidance or leading programming activities • 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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