Job Description
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 stat...