SAS/CDISC Statistical Programmer for Regulatory Submissions

Scorpion Therapeutics; Boston (MA); Hybrid; USD 120,000 - 170,000; Full time

Job summary

Scorpion Therapeutics is seeking a Statistical Programmer to support neuroendocrine clinical studies. The role focuses on developing and maintaining analysis datasets, tables, listings, and figures for study reports and regulatory submissions.

You will collaborate with Biostatistics, Data Management, and Clinical Development teams, ensuring CDISC standards and regulatory compliance. Some travel and a hybrid work setup in Boston are possible based on experience.

Qualifications

• MS in Statistics, Biostatistics, Mathematics, or related field.
• 3-5 years of SAS programming experience in biotech/pharma/CRO settings.
• Expertise in SAS, CDISC standards (SDTM, ADaM), and clinical trial reporting.

Responsibilities

• Develop, validate, and maintain analysis datasets, tables, listings, and figures for study reports and regulatory submissions.
• Collaborate with Biostatistics, Data Management, Clinical Development, and external vendors.
• Ensure compliance with CDISC standards and regulatory requirements.

Skills

SAS programming

CDISC standards

Prioritization

Education

MS in Statistics/ Biostatistics/ Mathematics

Tools

SDTM/ADaM

Job description

Scorpion Therapeutics is seeking a Statistical Programmer to support neuroendocrine clinical studies. The role focuses on developing and maintaining analysis datasets, tables, listings, and figures for study reports and regulatory submissions.

You will collaborate with Biostatistics, Data Management, and Clinical Development teams, ensuring CDISC standards and regulatory compliance. Some travel and a hybrid work setup in Boston are possible based on experience.