Senior Biostatistical Programmer

🔥 0 minutes ago

🔔 Pennsylvania – Remote

🔔 Pennsylvania – Remote

⏰ Full Time

🟠 Senior

🖥 Software Engineer

👻 Ghost score 10%

What it means: how likely this posting is sitting open without active hiring.How to read it: 60% or higher means we think this is a ghost. Lower scores are less of a worry.How we score it: age, reposts, open roles vs team size, how fast jobs close, and whether pay is listed.Fine print: an estimate from public data, not a judgment of the company. Real jobs can score high, so treat it as a hint, not a fact.

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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

• Design, develop, and validate SAS programs for statistical analysis and reporting of clinical trial data • Work closely with biostatisticians to create comprehensive analysis plans and apply appropriate statistical methods • Perform quality control checks and review statistical outputs for compliance with project specifications and regulatory guidelines • Assist in preparing statistical reports, presentations, and regulatory submissions supporting clinical development programs • Mentor junior programmers and contribute to team development by sharing best practices and technical knowledge • Analyze and report clinical trial data, ensuring the integrity and accuracy of statistical outputs

🎯 Requirements

• Bachelor's degree in statistics, computer science, mathematics, or a related discipline • Significant experience in statistical programming within the clinical research or pharmaceutical industry • Strong proficiency in SAS programming • Solid understanding of statistical concepts and methodologies • Excellent analytical skills and attention to detail • Ability to manage multiple projects simultaneously • Strong communication and interpersonal skills • Ability to work collaboratively within a multidisciplinary team • 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