Take on the role of Senior Statistical Programmer focused on oncology at IQVIA. Apply your robust SAS programming expertise to support clinical research initiatives. This position requires you to conduct essential statistical programming tasks using SAS Software, ensuring adherence to ICH guidelines and CDISC standards.

You'll generate analysis datasets and validate programs, working on multiple clinical studies with minimal supervision, while also reviewing validation outputs and documentation. Key Responsibilities:

- Conduct statistical programming and validate SAS outputs
- Generate analysis datasets in compliance with standards
- Assist in the preparation of analysis results and SAPs
- Review and clean validation summary reports
- Participate in TLF preparation and review Requirements:
- BA/BS in relevant field with equivalent experience
- 4-8 years of SAS programming in the pharmaceutical industry
- Robust organizational and communication skills
- Ability to manage time effectively under pressure
- Familiarity with regulatory guidelines and standards Bring your SAS expertise and attention to detail to elevate clinical research efforts at IQVIA.

📌 Clinical Statistical Programming Position at IQVIA (Mississauga)
🏢 IQVIA Argentina
📍 Mississauga