R/ SAS Programmer
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.
