SAS Programmer for Clinical Trials Development
2 months ago
Responsibilities:
• Develop and maintain high-quality SAS programs for clinical trials using CDISC standards (SDTM and ADaM).
• Collaborate with biostatisticians to design and implement statistical procedures for data analysis.
• Ensure thorough understanding of relational database components and theory for efficient data management.
• Apply strong application development skills to create innovative data solutions.
• Analyze clinical trial data and perform hands-on data manipulations, analysis, and reporting of results.
• Stay up-to-date with ICH E6, ICH E3, ICH E8, ICH E9, and clinical research processes.
• Adhere to department-specific and project standards and SOPs.
• Assist team members with day-to-day activities and act as an escalation point for programmers.
• Communicate effectively with sponsors for high-quality and on-time deliverables.
• Develop and recommend project standards and best practices.
• Troubleshoot complex data issues using SAS programming knowledge.
Requirements:
• Minimum 5+ years of experience in ADaM and TFL (SDTM experience is optional).
• Proficiency in Oncology TA, with experience working on ADTTE, ADRS, ADTU, ADTR datasets, and visualizations like KM Plots, Forest Plots, Swimmer lane plot, waterfall plot, etc.
• Strong understanding of RECIST Guidelines in Oncology.
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