SAS Programming Specialist
11 hours ago
We are looking for a talented SAS Programming Specialist to join our team at iQVIA Argentina. As a key member of our Clinical Programming group, you will be responsible for developing clinical study report materials according to the objectives of a clinical trial for regulatory submissions.
Key Responsibilities:
- Developing clinical study report materials according to the objectives of a clinical trial for regulatory submissions.
- Importing data from various sources and program quality control checks for source data and reporting data issues.
- Interpreting project-level requirements and developing programming specifications.
- Writing programming code following established Good Programming Practices.
- Programming ADaM datasets and creating statistical analysis tables, listings, and figures.
Requirements:
- A Master's or Bachelor's degree in Biostatistics, Statistics, Mathematics, or Computer Science.
- Strong educational or practical evidence in programming.
- Experience in programming in SAS within the CRO/Pharma/Biotech/Healthcare industries.
- Knowledge of statistics and exhibit routine and occasionally complex analytical skills.
- A focus on quality, accuracy, and completeness of work activities.
- Excellent communication skills.
Estimated Salary:$105,000 per year.
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