SAS Programmer for Clinical Trials Development

2 months ago


Shanghai, Shanghai, China IQVIA Full time

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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