Senior Statistical Programmer

Job not on LinkedIn

🔥 0 minutes ago

🌐 United Kingdom, France, +3 more countries – Remote

🇬🇧 United Kingdom – Remote 🇫🇷 France – Remote 🇪🇸 Spain – Remote 🇭🇷 Croatia – Remote 🇷🇴 Romania – Remote

⏰ Full Time

🟠 Senior

🖥 Software Engineer

Apply Now

Find Similar Remote Jobs

Set Up Email Alert For New Jobs

📊 Check your resume score for this job

Improve your chances of getting an interview by checking your resume score before you apply.

Upload Resume

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

• Analyse clinical trial data and support the statistical analysis process to ensure high-quality results • Lead statistical programming tasks requiring technical depth, with a focus on quality and continuous improvement • Develop and validate SAS programs for statistical analysis and reporting of clinical trial data • Collaborate with biostatisticians to define analysis plans and statistical methods for clinical data • Perform quality control checks on statistical outputs and ensure accuracy and consistency in reporting • Assist in preparing statistical reports, presentations, and publications for regulatory submissions • Contribute to process improvements by identifying efficiencies in programming practices and methodologies

🎯 Requirements

• Bachelor's degree in statistics, computer science, mathematics, or a related discipline • Experience in statistical programming, preferably in a clinical research or pharmaceutical setting • Strong proficiency in SAS programming • Solid understanding of statistical concepts and methodologies • Excellent analytical and problem-solving skills • Keen attention to detail • Strong communication skills • Ability to work collaboratively in a team environment • Ability to effectively convey complex information • 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 • Reasonable accommodations during the recruitment process