Statistical Programmer - Katalyst CRO : Job Details

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• Provide programming support for clinical trials within the pharmaceutical industry.
• Collaborate with Biostatisticians, Data Managers, and Clinical Research teams to develop and implement programming solutions for data analysis and reporting.
• Ensure the accuracy and consistency of clinical data.
• Develop, validate, and maintain SAS programs for data analysis and reporting.
• Create and document SAS programming standards and procedures.
• Perform data checks, quality control, and review activities.
• Prepare datasets for analysis, including merging and cleaning data.
• Prepare and review tables, listings, and figures for clinical reports.
• Ensure compliance with regulatory requirements and guidelines.
• Stay updated with new SAS programming methods and regulatory guidance.

• Bachelor's Degree in statistics, computer science, or a similar quantitative field.
• At least 5 years of clinical statistical programming experience in 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 and communication skills.
• Ability to collaborate effectively within a team.
• Knowledge of regulatory requirements for clinical trials and drug development.