Clinical SAS Programmer
Clinical SAS Programmer
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Salary Not Disclosed
1 Vacancy
Job Description
- Develop and maintain SAS programs to import clean and validate clinical trial data.
- Use R for data manipulation analysis and visualization.
- Perform statistical analyses in accordance with study protocols and analysis plans.
- Generate tables listings and figures (TLFs) using SAS and R.
- Create and QC statistical outputs and clinical study reports for regulatory submissions.
- Document programming activities and ensure compliance with Standard Operating Procedures (SOPs).
- Work closely with biostatisticians data managers and clinical researchers.
- Provide programming support for ad-hoc analysis requests and exploratory data analyses.
- Perform rigorous quality checks on all deliverables.
- Maintain annotated datasets and ensure traceability of data processing.
- Bachelors or masters degree in Statistics Computer Science Biostatistics or a related field.
- Minimum of 3 years of clinical SAS programming experience with a strong background in R.
- Proficiency in SAS and R including data step programming PROC SQL and R packages for data analysis.
- Experience with CDISC standards (SDTM ADaM).
- Knowledge of clinical trial processes and regulatory requirements (e.g. FDA EMA).
- Strong analytical and problem-solving skills.
- Excellent communication skills both written and verbal.
Employment Type
Full-time
