Statistical Programmer

Responsibilities

• Ensuring the accuracy and consistency of clinical data.
• Work closely with 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.
• Provide 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.

Requirements

• 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
• Ability to work in a team environment and collaborate effectively with other stakeholders