Principal Statistical Programmer

🔥 0 minutes ago

🌐 China, Taiwan – Remote

🇨🇳 China – Remote 🇹🇼 Taiwan – Remote

⏰ Full Time

🔴 Lead

🖥 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

• Manage day-to-day statistical programming activities, supporting the team to deliver quality outcomes • Lead the development and validation of statistical programs for data analysis and reporting, ensuring compliance with regulatory standards • Collaborate with biostatisticians and clinical teams to define project requirements and align with study objectives • Oversee the creation of programming specifications, documentation, and technical reports for regulatory submissions • Provide mentorship and guidance to junior statistical programmers • Stay current with industry trends and advancements in statistical programming to drive innovation and enhance project outcomes

🎯 Requirements

• Bachelor's degree in statistics, computer science, mathematics, or a related discipline • Significant experience in statistical programming, particularly in the context of clinical trials and regulatory submissions • Expertise in programming languages such as SAS, R, or Python, with proficiency in data management and statistical analysis • Excellent problem-solving skills and attention to detail, with a commitment to delivering high-quality results • Strong communication and interpersonal skills, facilitating effective collaboration across teams and with stakeholders • A commitment to maintaining high standards of quality and compliance in all 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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