Senior SAS Developer: Clinical Data Automation Lead

Certara; Germany (OH); On-site; USD 120,000 - 160,000; Full time

Job summary

Certara is seeking a Senior SAS developer to support Clinical Data Automation in a regulated life sciences environment. Strong SAS, R, and/or Python skills are required to design automated data workflows.

You will work with SDTM/ADaM datasets, Define.xml, and CDISC standards to ensure submission readiness and data quality across studies.

The role emphasizes reusable macros, automation frameworks, and collaboration with cross-functional teams to deliver scalable data solutions.

Qualifications

• 6+ years of Clinical trials SAS programming experience.
• Experience with Pinnacle 21 validation and Define.xml.
• CDISC SDTM/ADaM standards expertise.
• Define.xml creation and submission readiness.

Responsibilities

• Clinical Programming using SAS with R/Python as needed.
• Work with SDTM/ADaM datasets and Define.xml.
• Ensure CDISC standards for data standardization and validation.
• Develop reusable programming standards and automation frameworks.
• Collaborate with cross-functional teams to automate data quality checks.

Skills

SAS programming

R programming

Python programming

Clinical automation

CDISC SDTM/ADaM

Pinnacle 21

Data validation

Metadata-driven programming

Define.xml

APIs/workflows

Regulatory submission readiness

Macros/utilities

Data quality checks

Education

BSc/MSc Biostatistics or Life Sciences

Tools

Pinnacle 21 / P21 Enterprise

Job description

Certara is seeking a Senior SAS developer to support Clinical Data Automation in a regulated life sciences environment. Strong SAS, R, and/or Python skills are required to design automated data workflows.

You will work with SDTM/ADaM datasets, Define.xml, and CDISC standards to ensure submission readiness and data quality across studies.

The role emphasizes reusable macros, automation frameworks, and collaboration with cross-functional teams to deliver scalable data solutions.