Key Responsibilities

• Develop and maintain SAS programs for generating ADaM datasets and TFLs.
• Perform quality control and validation on programs developed by others.
• Collaborate with statisticians and data managers to ensure data accuracy and consistency.
• Create and maintain programming specifications and supporting documents.
• Participate in SOP/WPD compliance and continuous process improvement initiatives.
• Support ad-hoc data requests, clinical data reviews, and data validation activities.
• Continuously improve programming and clinical trial knowledge through training and mentoring.

Qualifications

• Bachelor’s or above in Statistics, Biostatistics, Mathematics, Computer Science, or related field.
• 1–2 years of SAS programming experience in clinical trials (pharma or CRO preferred).
• Strong understanding of clinical trial statistics and regulatory guidelines.
• Ability to work independently on assigned projects.
• Proficiency in Microsoft Office and statistical software.
• Good communication skills in English (written and spoken).
• Strong teamwork and documentation skills.