Senior SAS Programmer for Oncology Trials & Regulatory

Scorpion Therapeutics; New York (NY); On-site; USD 120,000 - 170,000; Full time

Job summary

Scorpion Therapeutics is seeking a Principal Statistical Programmer to provide expert-level SAS programming support for clinical trial data analysis and reporting in line with SAPs, ICH guidelines, and FDA requirements.

You will lead production of tables, listings, and figures for regulatory submissions and HEOR analyses, collaborating with statisticians, data managers, and cross-functional teams across multiple drug programs. Oncology experience is essential.

Qualifications

• At least 8 years relevant experience (5+ years may be considered); Bachelor’s degree.
• Oncology experience required; leukemia experience preferred.
• Excellent communication to non-technical colleagues and ability to manage multiple projects with aggressive timelines.
• Advanced SAS knowledge; familiar with WHO, MedDRA coding dictionaries; expert in CDISC.
• Knowledge of medical/statistical terminology; proficient with Windows, Word, and Excel.

Responsibilities

• Produce tables, listings, and figures and CRF tabulations (including ISS/ISE).
• Primary programmer for regulatory, commercial, ad hoc, biomarker, and HEOR analyses.
• Review Standards Artifacts and Processes (SAPs, Data Validation Plans, eCRFs) and provide comments.
• Troubleshoot and quality-review complex SAS programs and document work.
• Follow FDA regulations affecting clinical trial data reporting.

Skills

SAS programming

Regulatory knowledge

CDISC

Statistical terminology

Communication skills

Education

Bachelor’s degree

Tools

SAS

Microsoft Word/Excel

WHO/MedDRA coding dictionaries

CDISC standards

Windows

Job description

Scorpion Therapeutics is seeking a Principal Statistical Programmer to provide expert-level SAS programming support for clinical trial data analysis and reporting in line with SAPs, ICH guidelines, and FDA requirements.

You will lead production of tables, listings, and figures for regulatory submissions and HEOR analyses, collaborating with statisticians, data managers, and cross-functional teams across multiple drug programs. Oncology experience is essential.