Clinical SAS/R Programmer - Expert In Recruitment Solutions

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.