Found Description
Drive innovative statistical analysis as a Lead Statistical Analyst I, utilizing SAS for data management and programming standards. Join a dynamic team to enhance efficiency and compliance in clinical trials.
We are seeking a Senior Statistical Analyst I with a robust background in SAS programming within pharmaceutical or CRO settings. You will be responsible for developing complex analysis datasets and standard macros, thereby improving project delivery timelines. As a project lead, you'll mentor junior members, ensure ICH-GCP, and CDISC compliance, and communicate effectively with clients to manage deliverables and feedback.
Key Responsibilities:
• Develop complex analysis datasets (ADaM) using SAS
• Write programming specifications and documentation
• Create standard macros to enhance programming efficiency
• Lead project timelines and tasks for programming teams
• Conduct SAS code reviews and ensure quality standards
Requirements:
• Bachelor’s degree in S...
We are seeking a Senior Statistical Analyst I with a robust background in SAS programming within pharmaceutical or CRO settings. You will be responsible for developing complex analysis datasets and standard macros, thereby improving project delivery timelines. As a project lead, you'll mentor junior members, ensure ICH-GCP, and CDISC compliance, and communicate effectively with clients to manage deliverables and feedback.
Key Responsibilities:
• Develop complex analysis datasets (ADaM) using SAS
• Write programming specifications and documentation
• Create standard macros to enhance programming efficiency
• Lead project timelines and tasks for programming teams
• Conduct SAS code reviews and ensure quality standards
Requirements:
• Bachelor’s degree in S...
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