Make an impact with IQVIA as a Senior SAS Programmer specializing in clinical data analysis. This full time role in Durham requires expertise in programming and compliance with industry standards.

At IQVIA, you will leverage your 4-8 years in the pharmaceutical domain to conduct statistical programming using SAS Software. You’ll be responsible for generating analysis datasets, validating outputs, and ensuring all protocols align with ICH guidelines while performing ad-hoc analyses for product effectiveness.

Key Responsibilities:
• Conduct programming of clinical data using SAS Software
• Generate datasets that comply with CDISC standards
• Validate and review programming outputs from colleagues




• Assist in TLF shell preparation and SAP documentation
• Run CDISC validation programs to ensure compliance

Requirements:
• Bachelor’s degree in mathematics, statistics, or related fields
• 4-8 years of SAS programming experience in pharmaceuticals
• Exceptional attention to detail and organizational skills
• Knowledge of regulatory compliance and guidelines
• Capability to manage diverse tasks simultaneously

Utilize your SAS programming proficiency to drive impactful research outcomes at IQVIA.
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📌 IQVIA SAS Programmer – Clinical Data Focus (Ontario)
🏢 IQVIA
📍 Ontario