Company Overview

Our client is a leading global Contract Research Organization (CRO) dedicated to accelerating drug development and improving patient outcomes. With a growing presence across Europe and a reputation for delivering high-quality biometrics solutions, they partner with top pharmaceutical and biotech companies on innovative clinical trials across multiple therapeutic areas.

The Role

We are seeking Senior Statistical Programmers to join the biometrics team in permanent positions across Europe. This role involves working on diverse clinical trial projects, contributing to regulatory submissions, and collaborating with cross-functional teams to ensure data integrity and compliance.

Key Responsibilities

• Develop and validate SAS and/or R programs for clinical trial data analysis and reporting

• Create and maintain SDTM and ADaM datasets, TFL outputs, and submission packages in line with CDISC standards

• Support regulatory submissions by preparing high-quality deliverables

• Collaborate with biostatisticians, data managers, and clinical teams to ensure accurate and timely outputs

• Troubleshoot programming issues and provide technical guidance to junior team members

Qualifications

• Proven experience as a Statistical Programmer in clinical trials

• Strong proficiency in SAS and/or R programming

• Hands-on experience with CDISC standards (SDTM, ADaM) and TFL generation

• Familiarity with regulatory submission requirements

• Excellent communication and problem-solving skills

• Ability to work independently and as part of a global team

The Offer

• Competitive salary and benefits package

• Opportunity to work on global projects across multiple therapeutic areas

• Career development programs and continuous learning opportunities

• Collaborative and inclusive work environment focused on innovation

Send us your CV below and let us know why you would be a great fit for the opportunity.