Senior Statistical Programmer – R Programming

Job not on LinkedIn

🕒 August 19

🇵🇭 Philippines – Remote

⏰ Full Time

🟠 Senior

🖥 Software Engineer

👻 Ghost score 23%

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

• Develop and validate SAS programs for statistical analysis and reporting of clinical trial data • Collaborate with biostatisticians to define analysis plans and statistical methods • Perform quality control checks on statistical outputs • 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 • Lead statistical programming tasks requiring technical depth • Support the statistical analysis process for clinical trial data

🎯 Requirements

• Bachelor's degree in statistics, computer science, mathematics, or a related discipline • At least 3 years of experience in statistical programming, preferably in a clinical research or pharmaceutical setting • Strong proficiency in SAS programming • Solid understanding of statistical concepts and methodologies • At least basic proficiency in R programming applied in clinical research studies • Excellent analytical and problem-solving skills, with a keen attention to detail • Strong communication skills and ability to work collaboratively in a team environment • Must be amenable to work in a homebased setup • Legal right to work in the Philippines

🏖️ 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