SAS/R Programmer - Saxon Global : Job Details

Remote SAS/R Programmer contract role for a biopharma client. We are seeking a highly skilled Clinical SAS Programmer with strong R programming experience to join our dynamic team. This role will involve working with clinical trial data, performing statistical analysis, and generating comprehensive reports to support clinical research and regulatory submissions.**Key Responsibilities:**1. **Data Management:** - Develop and maintain SAS programs to import, clean, and validate clinical trial data. - Use R for data manipulation, analysis, and visualization.2. **Statistical Analysis:** - Perform statistical analyses in accordance with study protocols and analysis plans. - Generate tables, listings, and figures (TLFs) using SAS and R.3. **Report Generation:** - Create and QC statistical outputs and clinical study reports for regulatory submissions. - Document programming activities and ensure compliance with Standard Operating Procedures (SOPs).4. **Collaboration:** - Work closely with biostatisticians, data managers, and clinical researchers. - Provide programming support for ad-hoc analysis requests and exploratory data analyses.5. **Quality Assurance:** - Perform rigorous quality checks on all deliverables. - Maintain annotated datasets and ensure traceability of data processing.**Qualifications:**- **Education:** Bachelor's or Master's degree in Statistics, Computer Science, Biostatistics, or a related field. - **Experience:** Minimum of 3 years of clinical SAS programming experience, with a strong background in R. - **Technical Skills:** - 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). - **Soft Skills:** - Strong analytical and problem-solving skills. - Excellent communication skills, both written and verbal.