Statistical Programmer SCE Administrator (Biotechnology, Onsite)

Job summary

The role focuses on maintaining and improving a Statistical Computing Environment (SCE) and shared programming assets, ensuring stability and compliance. Responsibilities include managing SAS macro libraries, supporting R usage, and overseeing testing and user acceptance processes.

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 user acceptance testing, including defect management.
• Several years of experience in clinical development with a strong grasp of clinical trial data and compliance expectations.
• Familiarity with R and experience in R package management and reproducibility practices.
• Ability to work independently while effectively collaborating with various stakeholders.

Responsibilities

• Maintain and govern shared SAS macro libraries, including versioning and controlled deployment.
• Produce clear, audit-ready documentation such as user guides and change logs for the SCE.
• Plan and execute testing and user acceptance for updates, including defect tracking.
• Provide operational support for the SCE, including access coordination and troubleshooting.
• Collaborate with Biometrics and external partners to ensure consistent processes for shared assets.

Skills

• Strong attention to detail and a structured, quality-minded approach.
• Excellent documentation skills with a focus on clarity and compliance.
• Service-oriented mindset with the ability to coordinate with multiple stakeholders.

Education

• Relevant degree in a related field, with a focus on statistical programming or clinical development preferred.

Tools

• Proficient in SAS and R programming environments, with experience in documentation and testing tools.