Description

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.