Senior Statistical Analyst – RWE, SAS Programming

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🔥 0 minutes ago

🏄 California, Illinois, +12 more states – Remote

🏄 California – Remote 🌽 Illinois – Remote 🌾 Iowa – Remote 🌪️ Kansas – Remote 🐎 Kentucky – Remote 🗽 New York – Remote 🌲 North Carolina – Remote 🌲 Oregon – Remote 🍂 Massachusetts – Remote 🔔 Pennsylvania – Remote 🌴 South Carolina – Remote 🎸 Tennessee – Remote 🤠 Texas – Remote ⛷️ Utah – Remote

⏰ Full Time

🟠 Senior

🧐 Analyst

👻 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 and validate analysis datasets, tables, listings and figures • Take ownership of clinical research deliverables and apply expertise to complex challenges • Apply programming standards and specifications consistently • Perform quality control and resolve data or programming issues • Collaborate with biostatistics, data management and clinical stakeholders • Maintain traceable programming documentation and submission readiness • Provide technical guidance, peer review or mentoring on complex work within the discipline

🎯 Requirements

• Degree in statistics, mathematics, computer science or related quantitative discipline, or equivalent relevant programming expertise • Minimum of 5 years of experience in statistical analysis within the pharmaceutical, biotechnology, or CRO industry • Proficiency in statistical software SAS (R or Python are also used in a more limited capacity) • Understanding of clinical trial design, statistical methodologies, and regulatory requirements • Practical statistical programming experience in clinical trials using SAS or another appropriate statistical programming environment • Knowledge of CDISC SDTM and ADaM standards • Understanding of clinical trial data, statistical outputs and validation practices • Experience developing and validating analysis datasets, tables, listings and figures • Experience reviewing colleagues’ work and providing technical guidance on clinical statistical programming • Employment contingent upon having the 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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