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SAS Programmer - PMTS, Inc
Software Engineer
Senior SAS Programmer delivering FDA‑compliant clinical trial datasets, tables, listings, and analyses for medical product development, leveraging CDISC standards and advanced data analytics.
About the role
Key Responsibilities
- Develop, validate, and maintain SAS programs to generate CDISC‑compliant clinical trial datasets, statistical tables, listings, and figures.
- Collaborate with biostatisticians, data managers, and regulatory teams to ensure accurate and timely deliverables.
- Perform data quality checks, troubleshoot issues, and implement solutions to support FDA‑regulated product development.
- Document programming logic, maintain version control, and produce detailed technical reports.
- Participate in cross‑functional meetings to review study protocols, data specifications, and regulatory requirements.
Requirements
- 5+ years of SAS programming experience in a clinical research environment.
- Strong knowledge of CDISC standards (SDTM, ADaM, SEND) and FDA submission processes.
- Proficiency in data manipulation, statistical analysis, and report generation using SAS.
- Excellent problem‑solving skills and attention to detail.
- Effective communication and teamwork abilities in a regulated setting.