Biostatistician II

🔥 23 hours ago

🌐 United States, Mexico – Remote

🇺🇸 United States – Remote 🇲🇽 Mexico – Remote

🔔 Pennsylvania – Remote

🔔 Pennsylvania – Remote

⏰ Full Time

🟢 Junior

🧪 Clinical Research

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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

• Serve as lead biostatistician for programs of studies, or on simple to complex individual studies • Oversee statistical activities that support ICON’s interactions with clients and regulatory agencies • Review and approve statistical methods sections of study protocols • Author statistical analysis plans (SAPs) and statistical input to reports • Program using SAS and/or R for inferential statistics • Conduct statistical analyses for clients

🎯 Requirements

• Master's degree OR Ph.D in Biostatistics, Statistics, or a related field • 1+ years of biostatistical experience in either a CRO, pharmaceutical, or biotech company • In-depth knowledge of study designs, and statistical analysis conventions in one or more therapeutic areas • Knowledge of clinical trials methodology, regulatory requirements, statistics and statistical software packages, including SAS • Experience working in a clinical research organization (preferred) • Effective written and verbal communication skills with demonstrated leadership ability • Ability to prioritize with strong time management skills • 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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