Senior Statistical Programmer

Skills Alliance; Netherlands; Hybrid; EUR 55,000 - 75,000; Full time

Benefits offered by this job

Pension scheme

Generous annual leave allowance

Opportunities for professional growth

Job summary

Skills Alliance is seeking an experienced Senior Statistical Programmer to join their team in the Netherlands. In this flexible hybrid role, you will contribute to statistical programming and reporting for clinical studies using SAS.

The ideal candidate will have 3–5+ years of experience, proficiency in SAS, and the ability to work within regulated environments. Offering permanent employment with competitive salary and benefits, this position is perfect for those looking to grow in the life sciences industry.

Qualifications

• 3–5+ years of statistical programming experience within life sciences or clinical research.
• Proficiency in SAS Base and SAS Macro.
• Understanding of regulated environments and data quality expectations.

Responsibilities

• Statistical programming and reporting for clinical studies.
• Development and maintenance of SAS programs and macros.
• Collaboration with cross‑functional and international teams.

Skills

SAS Base

SAS Macro

CDISC standards

Statistical programming

Regulated environments

Job description

We are looking for an experienced Senior Statistical Programmer to join a growing team supporting clients within the life sciences sector on a permanent basis.

In this role, you will contribute to the analysis, reporting, and programming activities for clinical and pre‑clinical studies using SAS. You will work with a range of international clients across pharmaceuticals, medical devices, biotechnology, and related industries.

This is a flexible hybrid opportunity, offering a combination of remote working, office collaboration, and occasional client‑site engagement.

Key Responsibilities

• Statistical programming and reporting for clinical studies
• Development and maintenance of SAS programs and macros
• Working within regulated environments and quality standards
• Collaboration with cross‑functional and international teams
• Delivery of projects within agreed timelines

Requirements

• Strong experience with SAS Base and SAS Macro
• Experience working with CDISC standards
• 3–5+ years of statistical programming experience within life sciences or clinical research
• Understanding of regulated environments and data quality expectations
• Professional proficiency in English
• Proactive, independent, and collaborative working style
• SAS certification or willingness to obtain certification preferred

What’s on Offer

• Permanent employment opportunity (full‑time or part‑time options available)
• Competitive salary and benefits package
• Flexible hybrid working model
• Pension scheme and generous annual leave allowance
• International and collaborative work environment
• Opportunities for professional growth and long‑term career development

If you are interested in joining a collaborative and quality‑driven consulting environment within the life sciences industry, feel free to get in touch.