Job Description

• The SAS/Statistical Programmer will also be responsible for ensuring the accuracy and consistency of clinical data.
• The successful candidate will work closely with the Biostatisticians, Data Managers, and Clinical Research teams to develop and implement programming solutions to support clinical data analysis and reporting
• Develop and validate SAS programs to support clinical trial data analysis and reporting
• Create, maintain, and document SAS programming standards and procedures
• Collaborate with Biostatisticians, Data Managers, and Clinical Research teams to ensure programming requirements are met
• Perform data checks, quality control checks, and data review activities to ensure data accuracy and consistency
• The SAS/Statistical Programmer will be responsible for providing programming support for clinical trials conducted within the pharmaceutical industry
• Prepare datasets for analysis, including merging and cleaning data from various sources
• Prepare and review tables, listings, and figures for clinical study reports
• Ensure compliance with regulatory requirements and guidelines
• Keep up to date with new SAS programming methods and software, as well as regulatory guidance

• Bachelor's Degree in statistics, computer science, or a similar quantitative field
• 4+ years of clinical statistical programming experience within the pharmaceutical or related industry
• Proficiency in SAS programming
• Knowledge of CDISC data standards
• Strong attention to detail and ability to work independently
• Excellent problem-solving skills
• Excellent verbal and written communication skills
• Knowledge of regulatory requirements for clinical trials and drug development
• bility to work in a team environment and collaborate effectively with other stakeholders

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