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Job Description & How to Apply Below
In this role, you will be responsible for the development and validation of complex datasets, leading programming initiatives, and mentoring junior programmers. You'll communicate regularly with clients, ensuring the delivery of precise outputs while adhering to ICH-GCP and CDISC standards. Your involvement in code reviews will enhance quality and compliance in programming deliverables.
Key Responsibilities:
• Validate complex analysis datasets and TFLs with SAS
• Write programming specifications and documentation
• Develop standard macros for operational efficiency
• Lead programming projects and mentor junior team members
• Manage client communications and feedback processes
Requirements:
• Bachelor’s degree in Statistics, Mathematics, or related field
• 5+ years of SAS programming experience in pharmaceuticals
• Strong knowledge of regulatory requirements and statistical methods
• Proven experience in leading programming projects
• Excellent communication abilities for working with global teams
Utilize your statistical expertise and SAS proficiency to contribute to high-impact clinical projects.
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Position Requirements
10+ Years
work experience
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