Senior Statistical Programmer

Scorpion Therapeutics; Boston (MA); Hybrid; USD 120,000 - 160,000; Full time

Job summary

Scorpion Therapeutics seeks a Senior Statistical Programmer to support biostatistics activities in clinical development for a rare neuroendocrine disease biopharma. You will deliver analysis datasets, tables, listings, figures and assist regulatory submissions.

The role requires an MS in Statistics/Biostatistics and 3+ years of SAS programming experience in biotech/pharma/CRO settings, with CDISC standards expertise. Hybrid work model in Boston with potential travel may apply.

Qualifications

• MS in Statistics, Biostatistics, or related field.
• 3+ years of SAS programming experience in biotech/pharma/CRO settings.
• Strong knowledge of CDISC SDTM/ADaM standards and trial analysis.

Responsibilities

• Lead or support programming for clinical studies.
• Develop and maintain SDTM/ADaM specifications and datasets.
• Ensure regulatory compliance and collaborate with Biostatistics, Data Management, Clinical Development, and Regulatory Affairs.

Skills

SAS programming

Clinical trial analysis

R (preferred)

Education

MS in Statistics/Biostatistics

Tools

CDISC standards

Job description

Role

Senior Statistical Programmer supporting biostatistics activities in clinical development for a rare neuroendocrine disease biopharma. Objectives include delivering analysis datasets, tables, listings, figures, and supporting regulatory submissions.

Responsibilities

Responsibilities encompass leading or supporting programming for clinical studies, developing and maintaining SDTM/ADaM specifications, ensuring regulatory compliance, and collaborating with cross-functional teams such as Biostatistics, Data Management, Clinical Development, and Regulatory Affairs.

Qualifications

Qualifications include an MS in Statistics, Biostatistics, or related fields, with 3+ years of SAS programming experience in biotech/pharma/CRO settings, and expertise in CDISC standards and trial analysis.

Preferred Skills

Preferred skills involve experience with R or modern tools, vendor oversight, and supporting study-level and integrated analyses (e.g., ISS/ISE).

Location and Working Arrangement

The position is based in Boston, MA, operating under a hybrid-work model, with potential travel.

Role Context

The role involves work within the regulatory stage, supporting INDs, regulatory submissions, and clinical trial reporting in a GxP environment.