onsite
Experienced ICL Programmer - J&J Family of Companies
Software Engineer
Senior ICL programmer responsible for designing, developing, and validating clinical data workflows using SAS, Python, and SQL to support complex medical studies and regulatory submissions.
About the role
Key Responsibilities
- Develop and maintain ICL scripts for clinical data extraction, transformation, and loading across multiple study sites.
- Collaborate with biostatisticians and data managers to ensure data integrity and compliance with regulatory standards.
- Perform data validation, quality checks, and troubleshooting to resolve discrepancies in study datasets.
- Document programming logic, create detailed technical specifications, and maintain version control using Git.
- Support the creation of study reports, tables, and figures for regulatory submissions.
Requirements
- 5+ years of experience in clinical programming, preferably within ICL environments.
- Strong understanding of clinical trial processes, CDISC standards, and regulatory submission requirements.
- Excellent problem‑solving skills and attention to detail.
- Effective communication skills and ability to work collaboratively in cross‑functional teams.