Senior SAS Developer

Scorpion Therapeutics; United States; On-site; USD 110,000 - 150,000; Full time

Job summary

Scorpion Therapeutics is seeking a Senior SAS developer to support Clinical Data Automation within biopharma clinical trial environments. You will develop, validate, and maintain automated workflows for clinical data standardization and submission-readiness.

Responsibilities include designing data pipelines for SDTM, ADaM, and Define.xml, applying CDISC standards, and integrating with Pinnacle 21 systems. You will build reusable automation utilities and collaborate cross-functionally to optimize

Qualifications

• BSc/ MSc in Biostatistics, Bioinformatics, or related field.
• 6+ years in clinical programming for drug development.
• Extensive SAS, CDISC standards, Pinnacle 21, and clinical trial data experience.
• Familiarity with R or Python is a plus; strong communication skills.

Responsibilities

• Design data pipelines for SDTM, ADaM, and Define.xml with CDISC standards.
• Apply CDISC standards and integrate with P21 systems; build reusable automation utilities.
• Collaborate cross-functionally to optimize clinical data processes.
• Develop, validate, and maintain automated workflows for data standardization and submission readiness.

Skills

SAS programming

CDISC standards

Pinnacle 21

Clinical data standards

Python

R

Data pipelines

Cross-functional collaboration

Education

Biostatistics/Bioinformatics

Tools

Pinnacle 21

Job description

Role:

Senior SAS developer supporting Clinical Data Automation within biopharma clinical trial environments. Objectives include developing, validating, and maintaining automated workflows for clinical data standardization, validation, and submission-readiness.

Responsibilities:

encompassing designing data pipelines for SDTM, ADaM, and Define.xml, applying CDISC standards, and integrating with P21 systems; building reusable automation utilities; and collaborating cross-functionally to optimize data processes.

Requirements:

B.Sc./M.Sc. in Biostatistics, Bioinformatics, or related; 6+ years in clinical programming for drug development; extensive experience with SAS, CDISC standards, Pinnacle 21, and clinical trial data structures; familiarity with R or Python is a plus; strong communication skills.

HighValue:

expertise in clinical data validation, automated data flow design, regulatory submission standards, and metadata-driven programming.

WorkSetup:

not specified, but likely in a regulated, collaborative clinical environment.