Statistical Programmer SCE Administrator (Biotechnology, Onsite)

Job summary

The role focuses on managing a Statistical Computing Environment (SCE) and ensuring the stability and documentation of shared programming assets. Responsibilities include maintaining SAS macro libraries, supporting R usage, and ensuring compliance with GxP standards through structured testing and user acceptance testing (UAT).

Qualifications

• Extensive experience in SAS programming, particularly in macro development and maintenance.
• Proven track record in creating and maintaining technical documentation for regulated processes.
• Hands-on experience with test planning, execution, and UAT, including defect management.
• Several years of experience in clinical development with a solid understanding of clinical trial data and compliance expectations.
• Familiarity with R and experience in managing R packages and reproducible workflows.
• Ability to work independently while collaborating with various stakeholders and external partners.

Responsibilities

• Maintain and govern shared SAS macro libraries, including versioning and controlled deployment.
• Produce clear, audit-ready documentation for the SCE and shared code assets.
• Plan and execute testing and UAT for updates, including defect tracking.
• Provide operational support for the SCE, including access coordination and troubleshooting.
• Support the use of R in the SCE, focusing on package management and reproducibility.
• Collaborate with internal teams and external partners to ensure consistent processes.

Skills

• Strong attention to detail and a structured approach to documentation and processes.
• Quality-minded with a service-oriented attitude.
• Ability to coordinate changes and testing with multiple stakeholders.

Education

• Relevant degree in a related field, with experience in clinical development.

Tools

• Proficient in SAS and R programming languages.