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Statistical Programmer I - Everest Clinical Research
Software Engineer
Entry‑level statistical programmer supporting clinical trial data preparation, transformation, and analysis using SAS, R, and Python while adhering to CDISC standards for regulatory submissions.
About the role
Key Responsibilities
- Develop and maintain SAS programs to create SDTM and ADaM datasets from raw clinical trial data.
- Perform data validation, cleaning, and quality checks to ensure compliance with CDISC standards.
- Collaborate with biostatisticians and data managers to support statistical analysis plans and generate tables, listings, and figures.
- Document programming processes, create metadata, and maintain traceability for regulatory submissions.
- Assist in the preparation of deliverables for FDA, EMA, and other health authority submissions.
Requirements
- Bachelor’s degree in Statistics, Biostatistics, Computer Science, or related field.
- Proficiency in SAS programming; exposure to R or Python is a plus.
- Understanding of CDISC standards (SDTM, ADaM) and clinical trial data structures.
- Strong analytical and problem‑solving skills with attention to detail.
- Effective communication and ability to work in a cross‑functional team environment.