Senior SAS Programmer – Clinical Trials (Contract)

Soho Square Solutions; Irvine (CA); On-site; USD 110,000 - 150,000; Full time

Job summary

Soho Square Solutions in Irvine, CA is seeking a Statistics & Statistics Programming Specialist 3 for a 6-month contract on site. The Senior Statistical Programmer – Contractor will develop and validate analysis datasets and outputs for clinical studies, collaborating with Biostatistics and Clinical Data Management.

You will create, modify, and validate SAS programs to produce tables, listings, and figures, ensuring inspection-ready documentation.

Qualifications

• 8+ years of relevant statistical programming experience or 6+ years with a master’s degree
• Experience with SAS programming for clinical trials and CDISC standards (SDTM/ADaM)
• Experience developing tables, listings, and figures; regulatory submissions experience

Responsibilities

• Develop complex analysis datasets, specifications, and summary outputs (tables, listings, figures) for clinical study reports, regulatory submissions, and internal presentations
• Create, modify, and maintain SAS programs that meet regulatory and company standards to ensure efficient programming, reporting, review, and traceability
• Perform independent program review and validation with inspection-ready documentation
• Support ad hoc analyses in collaboration with the designated statistician and data management team
• Review CRFs and database specifications with the study team; identify risks and communicate them clearly

Skills

SAS programming

SAS Base

SAS/STAT

SAS Macros

CDISC SDTM/ADaM

Regulatory knowledge (GCP/ICH/FDA/ISO)

R or Python

Cross-functional collaboration

Data management collaboration

Education

Bachelor’s degree in Statistics/Math/CS

Master’s degree in a related field

Tools

SAS software

Microsoft Excel

Microsoft Word

PowerPoint

Job description

Soho Square Solutions in Irvine, CA is seeking a Statistics & Statistics Programming Specialist 3 for a 6-month contract on site. The Senior Statistical Programmer – Contractor will develop and validate analysis datasets and outputs for clinical studies, collaborating with Biostatistics and Clinical Data Management.

You will create, modify, and validate SAS programs to produce tables, listings, and figures, ensuring inspection-ready documentation.