Lead Oncology SAS Programmer – CDISC & Analysis

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

Job summary

IQVIA is seeking a SAS programmer in the United States (Durham, NC area) to perform statistical programming for clinical data in accordance with ICH guidelines and SOPs. You will develop analysis datasets per CDISC standards, create tables and graphs, and support SAP preparation with minimal supervision.

The role requires 4–8 years of SAS experience in pharma, strong attention to detail, and the ability to manage multiple tasks under tight timelines.

Qualifications

• BA/BS in math, statistics, CS or health field, or equivalent experience.
• 4–8 years of SAS programming in pharma.
• Strong SAS skills and meticulous attention to detail.
• Knowledge of regulatory guidelines including electronic submission standards.
• Strong organizational, communication, and leadership skills.
• Ability to work under tight deadlines and handle multiple tasks.

Responsibilities

• Conduct statistical programming on clinical data using SAS.
• Ensure programs, outputs, and docs follow ICH guidelines and SOPs.
• Create analysis datasets per CDISC standards and SAP.
• Produce summary tables, graphs, and listings; perform adhoc analyses.
• Validate programs and outputs created by colleagues.
• Assist in SAP preparation and TLF shell review.
• Run CDISC validation (OpenCDISC) to ensure ADaM CDISC compliance.
• Learn and implement Incyte SAS macros for efficiency.
• Program independently for studies with minimal supervision.
• Check validation summary reports for errors and proper docs.
• Review CDISC validation output for each study.

Skills

SAS programming

CDISC standards

Regulatory knowledge

Leadership

Time management

Communication

Attention to detail

Education

BA/BS in math, statistics, CS or health

Tools

SAS

OpenCDISC

Job description

IQVIA is seeking a SAS programmer in the United States (Durham, NC area) to perform statistical programming for clinical data in accordance with ICH guidelines and SOPs. You will develop analysis datasets per CDISC standards, create tables and graphs, and support SAP preparation with minimal supervision.

The role requires 4–8 years of SAS experience in pharma, strong attention to detail, and the ability to manage multiple tasks under tight timelines.