Lead Statistical Programmer – Global Trials (Barcelona)

AstraZeneca plc; Barcelona; On-site; EUR 120,000 - 150,000; Full time

Job summary

AstraZeneca plc in Barcelona is seeking a Senior Statistical Programmer to lead programming for clinical studies across global trials. Based on-site three days per week, the role combines scientific rigor with data-driven programming to deliver analysis-ready datasets and outputs.

You will collaborate with statisticians, lead programmers, data managers and study leaders, ensure CDISC standards, automate workflows, and influence study strategies while meeting regulatory expectations.

Qualifications

• Degree in Mathematics, Statistics, Computer Science, Life Science or equivalent.
• Excellent programming skills in SAS (or R) and SAS macros.
• Proficient knowledge of the clinical development process and CDISC.
• Ability to apply programming knowledge to problem solving.
• Ability to manage relevant documentation.
• Ability to influence stakeholders on Programming items.
• Current knowledge of technical and regulatory requirements.

Responsibilities

• Lead programming deliverables for clinical studies or small to medium projects.
• Deliver high-quality outputs on schedule with compliant standards.
• Implement programming aspects of protocols and development plans.
• Program independently with efficiency and precision.
• Write clear programming specifications and audit-ready documentation.
• Adhere to CDISC standards and promote automation.
• Collaborate with statisticians, lead programmers and data managers.
• Identify and manage programming risks proactively.

Skills

SAS programming

R

SAS macros

Problem solving

Documentation

Stakeholder influence

Regulatory knowledge

Education

Math/Stats/CS or Life Science degree

Tools

SAS

R

Job description

AstraZeneca plc in Barcelona is seeking a Senior Statistical Programmer to lead programming for clinical studies across global trials. Based on-site three days per week, the role combines scientific rigor with data-driven programming to deliver analysis-ready datasets and outputs.

You will collaborate with statisticians, lead programmers, data managers and study leaders, ensure CDISC standards, automate workflows, and influence study strategies while meeting regulatory expectations.