Clinical Data Programmer

Overview

As a Clinical Data Programmer at Charles River, you will translate complex clinical data into production-ready datasets to support regulatory submissions. You will work remotely from the UK, collaborating with cross-functional teams to deliver SDTM/ADaM datasets and validated outputs that meet SOPs and regulatory standards. You’ll troubleshoot, optimize code, and mentor peers while driving data integrity and timely delivery in a fast-paced environment. This role offers the chance to shape clinical data workflows within a global leader in safety assessment and drug development.

Pay / Benefits

• bonus
• benefits
• salary range 30,000-34,000/annum
• remote work (UK)
• opportunity for career growth

Responsibilities

• Produce production clinical datasets using established systems and standardized code
• Develop reusable code aligned with requirements and SOPs for UAT datasets
• Prepare SDTM and/or ADaM datasets as needed
• Review data and code for integrity, accuracy, and protocol adherence
• Lead troubleshooting of generic or study-specific code and ensure data aligns with study documentation
• Maintain comprehensive study documentation, testing, and QC in line with regulatory guidelines
• Review Data Transfer Agreements and/or Specifications
• Communicate strategy, plans, and changes to stakeholders to ensure quality Deliverables
• Manage study schedules and coordinate internal and external resources
• Support application development and study code standardization
• Handle complex workloads with tight deadlines and multiple clients
• Mentor peers and junior staff in support of business needs
• Design and support systems that generate custom tables/graphs and enable business intelligence
• Research and advise on new technology; draft/update SOPs
• Function as team lead when needed and assist with administrative activities
• Perform additional related duties as assigned

Key requirements

• Bachelor’s degree in a scientific discipline
• Significant SAS experience in a regulated environment or clinical research setting
• Proficiency with SAS macros, arrays, SQL, SAS Graph, and output formats (.rtf, .xml, .xpt)
• Proficiency in another programming language (e.g., .NET, VBA) is a plus
• Familiarity with SDLC is a plus
• Strong organizational skills
• Basic familiarity with Microsoft Office Suite
• Ability to learn validated systems and work extended hours as needed
• Right to Work in the UK (no sponsorship)
• Knowledge of Data Transfer Agreements and regulatory compliance (implicit)

• strong communication
• mentoring and team collaboration
• time management under deadlines
• SAS programming
• SAS macros and arrays
• SQL

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