Senior Statistical Programmer – Oncology

IQVIA

. Conduct statistical programming work of clinical data using SAS Software .

Posted 9/16/2026full-timeDurham • North Carolina • United StatesSenior💰 $88,300 - $220,900 per yearWebsite

Core Competencies

Role fit

Core Competencies

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Proficient in SAS Programming for clinical data analysis, ensuring compliance with ICH guidelines and CDISC standards. Capable of managing multiple projects while maintaining attention to detail and effective communication.

Highest-signal resume keywords

SAS ProgrammingCDISC ComplianceStatistical AnalysisRegulatory Guidelines KnowledgeProject Coordination

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Statistical ProgrammingData AnalysisSAS SoftwareCDISC StandardsAnalysis Datasets GenerationSummary Tables ProductionGraph CreationAd Hoc AnalysesValidation ProgrammingSAS Macros Implementation

Soft Skills

Attention to DetailOrganizational SkillsTime ManagementCommunication SkillsLeadership Skills

Tools & Technologies

OpenCDISCSAS Software

Industry Keywords

Pharmaceutical IndustryICH GuidelinesSOPsSAP PreparationTLF Shell Preparation

About the role

Key responsibilities & impact

Conduct statistical programming work of clinical data using SAS Software
Ensure programs, outputs and documentation comply with ICH guidelines and company SOPs
Generate analysis datasets according to CDISC standard and SAP
Implement analysis methods according to SAP and produce summary tables, graphs and data listings using SAS
Conduct ad hoc analyses
Validate programs and associated results produced by other programming colleagues
Participate in TLF shell preparation and review
Assist statistician with SAP preparation
Run CDISC validation programs such as OpenCDISC reports to ensure ADaM datasets are CDISC compliant
Learn and implement Incyte standard SAS macros for efficient clinical-data analyses under Lead Programmer supervision
Independently program for individual studies with minimum supervision
Check validation summary reports for errors, warnings, and proper SAS-program documentation
Review individual study CDISC validation output

Requirements

What you’ll need

BA/BS degree in mathematics, statistics, computer science or health related field, or equivalent experience
4–8 years of SAS programming working experience in the pharmaceutical industry
Good SAS programming skills and attention to details
Demonstrated knowledge of regulatory guidelines, including electronic submission standards
Strong organizational, time management, communication, and project coordination and leadership skills
Must be able to work well under timeline pressure
Must be able to work on multiple tasks while coordinating others at the same time

Benefits

Comp & perks

Incentive plans, bonuses, and/or other forms of compensation may be offered
Health and welfare benefits may be offered
Other benefits may be offered