Join our team as a Lead SAS Programmer where you will contribute to impactful clinical trials by developing analysis datasets and leading programming efforts.

We're seeking a Senior Statistical Analyst with a strong background in SAS programming and at least three years of experience in a pharmaceutical or CRO setting. Your role will encompass validating ADaM datasets, creating efficient standard macros, and communicating effectively with clients and stakeholders.

Key Responsibilities: • Develop and validate ADaM datasets and TFLs using SAS • Write, review, and maintain programming specifications • Utilize standard macros to enhance programming workflows • Lead project timelines and guide junior team members • Conduct code reviews to ensure high-quality outputs

Requirements: • Bachelor's degree in Statistics, Mathematics, or similar field • Minimum 3 years SAS programming experience in relevant settings • Strong understanding of clinical trial requirements • Proven experience in leading programming projects • Excellent global communication abilities

Leverage your SAS expertise and leadership to drive excellence in statistical analysis. #J-18808-Ljbffr

📌 Lead SAS Programmer - Senior Statistical Analyst (Shubenacadie)
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📍 Shubenacadie