Senior SAS Programmer – Oncology (CDISC, SAP)

IQVIA Argentina; Durham (NC); On-site; USD 88,000 - 221,000; Full time

Job summary

IQVIA is a leading global provider of clinical research services and healthcare insights. This role focuses on statistical programming for clinical data, ensuring adherence to ICH guidelines and SOPs, and producing CDISC-compliant datasets and outputs.

The candidate will implement SAP-driven analysis methods, generate tables and listings, validate programs, and participate in SAP preparation and TLF reviews under supervision. Strong SAS skills and regulatory knowledge are essential.

Qualifications

• BA/BS degree in mathematics, statistics, computer science or health related field, or equivalent experience.
• 4–8 years of SAS programming experience in the pharmaceutical industry.
• Strong SAS programming skills with attention to detail.
• Knowledge of regulatory guidelines, including electronic submission standards.
• Strong organizational, time management, communication and leadership skills.

Responsibilities

• Conduct statistical programming work of clinical data using SAS Software.
• Ensure programs, outputs and documentation comply with ICH guidelines and SOPs.
• Generate analysis datasets per CDISC standard and SAP.
• Implement analysis methods and produce tables, graphs, and listings; conduct adhoc analyses.
• Validate programs and results produced by colleagues.
• Assist in SAP preparation and TLF shell reviews.
• Run CDISC validation programs (OpenCDISC) to ensure ADaM CDISC compliance.
• Learn and implement client SAS macros for efficient analyses under supervision.
• Program for individual studies with minimal supervision.
• Check validation summary reports for errors and proper documentation.
• Review study CDISC validation output.

Skills

SAS programming

CDISC standards

OpenCDISC validation

Regulatory guidelines knowledge

Project coordination

Education

BA/BS in mathematics/statistics/computer science/health related

Tools

SAS

Job description

IQVIA is a leading global provider of clinical research services and healthcare insights. This role focuses on statistical programming for clinical data, ensuring adherence to ICH guidelines and SOPs, and producing CDISC-compliant datasets and outputs.

The candidate will implement SAP-driven analysis methods, generate tables and listings, validate programs, and participate in SAP preparation and TLF reviews under supervision. Strong SAS skills and regulatory knowledge are essential.