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Statistical Programmer II - LivaNova
Software Engineer
Statistical Programmer II responsible for designing, developing, and validating statistical programs for clinical trials using SAS, R, and SQL, ensuring data integrity and compliance with regulatory standards.
About the role
Key Responsibilities
- Develop, test, and maintain SAS and R programs for clinical trial data analysis and reporting.
- Validate statistical outputs and ensure compliance with ICH GCP, FDA, and EMA guidelines.
- Collaborate with biostatisticians, data managers, and project teams to define data requirements and deliverables.
- Document programming logic, run reports, and troubleshoot data discrepancies.
- Participate in protocol development and statistical analysis plan creation.
Requirements
- 3+ years of experience in statistical programming within the clinical research industry.
- Experience with clinical trial data standards (CDISC SDTM, ADaM) and regulatory submissions.
- Excellent problem‑solving, communication, and documentation skills.
- Ability to work independently and in cross‑functional teams in a fast‑paced environment.