Senior Oncology SAS Programmer (CDISC)

IQVIA LLC; Durham, Northern (NC, KY); Hybrid; USD 88,000 - 221,000; Full time

Job summary

IQVIA is seeking an experienced SAS Programmer to conduct statistical programming for clinical data in Durham, NC. You will generate analysis datasets per CDISC standards, produce SAP tables, graphs and listings, and validate programs under tight timelines.

You will collaborate with Lead Programmers, learn Incyte macros, ensure compliance with ICH guidelines and SOPs, and help prepare TLF shells and SAP deliverables while handling multiple studies with minimal supervision.

Qualifications

• BA/BS degree in mathematics, statistics, computer science or health related field or equivalent experience.
• 4–8 years SAS programming in the pharmaceutical industry.
• Strong knowledge of regulatory guidelines and CDISC standards.

Responsibilities

• Conduct statistical programming using SAS; generate analysis datasets according to CDISC.
• Produce summary tables, graphs and data listings using SAS; perform adhoc analyses.
• Validate programs and results; review CDISC validation output.
• Participate in SAP preparation and TLF shell review.
• Learn and implement Incyte SAS macros; work with Lead Programmers.
• Work independently on studies with minimum supervision.
• Ensure validation reports are clean of errors and properly documented.

Skills

SAS programming

CDISC knowledge

SAS macros

Attention to detail

Time management

Communication skills

Leadership / coordination

Education

BA/BS in mathematics, statistics, computer science or health related field

Tools

OpenCDISC

SAS

Job description

IQVIA is seeking an experienced SAS Programmer to conduct statistical programming for clinical data in Durham, NC. You will generate analysis datasets per CDISC standards, produce SAP tables, graphs and listings, and validate programs under tight timelines.

You will collaborate with Lead Programmers, learn Incyte macros, ensure compliance with ICH guidelines and SOPs, and help prepare TLF shells and SAP deliverables while handling multiple studies with minimal supervision.