Senior SAS Programmer — CDISC, ICH Compliance Lead

IQVIA Argentina; Mississauga; On-site; CAD 123,000 - 308,000; Full time

Job summary

IQVIA in Mississauga, Canada, is seeking an experienced SAS Programmer to perform statistical programming for clinical data in accordance with ICH guidelines and SAP. You will generate analysis datasets, tables, graphs and listings, and validate outputs with senior staff while learning Incyte SAS macros.

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

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 and attention to detail.
• Knowledge of regulatory guidelines and electronic submission standards.
• Organizational, time management, communication, and leadership skills.
• Ability to multitask and work under tight timelines.

Responsibilities

• Develop SAS programs for clinical data according to CDISC standards and SAP.
• Create analysis datasets, tables, figures, and listings; perform adhoc analyses.
• Validate programs and results produced by colleagues.
• Contribute to SAP preparation and review of TLF shell.
• Ensure CDISC validation outputs are CDISC-compliant.
• Work with Lead programmers to implement Incyte SAS macros.
• Operate independently on multiple studies with minimal supervision.

Skills

SAS programming

Attention to detail

Time management

Communication

Leadership

Education

BA/BS in mathematics, statistics, CS or health-related field

Tools

SAS

Job description

IQVIA in Mississauga, Canada, is seeking an experienced SAS Programmer to perform statistical programming for clinical data in accordance with ICH guidelines and SAP. You will generate analysis datasets, tables, graphs and listings, and validate outputs with senior staff while learning Incyte SAS macros.

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