Business Head at Radiant Systems Europe Ltd | Leading Team Management Initiatives
R&D Programmer / Senior Statistical Programmer / Principal SAS Programmer / Lead Clinical SAS Programmer / Clinical Programming Manager
About the Role
We are seeking an experienced R&D Programmer (Clinical Programming Manager) to join our global clinical research team. This role is responsible for overseeing the programming components of clinical trials — ensuring the timely, accurate, and compliant delivery of data and analyses that support regulatory submissions and scientific publications.
You’ll lead cross-functional or outsourced teams, contribute to design and analysis planning, and help standardize programming deliverables across projects to drive quality and efficiency in clinical development.
Key Responsibilities
* Lead and manage programming activities across multiple clinical projects, ensuring delivery of high-quality datasets, tables, listings, and figures (T/L/G).
* Provide strong programming support for CDISC-based e-submissions, including SDTM and ADaM dataset development.
* Develop, review, and validate generic SAS macros to improve efficiency and standardization.
* Support the reporting and statistical analysis of clinical trial data, ensuring accuracy and compliance with regulatory requirements.
* Collaborate with cross-functional teams to develop programming strategies and process improvements.
* Oversee and mentor contingent workers or vendors; provide training as needed.
* Contribute to budget planning and project-level programming strategy.
Requirements
* Bachelor’s, Master’s, or PhD in Science, Statistics, Information Technology, or related discipline.
* Bachelor’s + 5 years or Master’s + 4 years of professional programming experience in the pharmaceutical or clinical research industry.
* Hands‑on experience with SDTM, ADaM, and CDISC standards.
* Strong proficiency in SAS programming, including developing and validating clinical datasets and statistical outputs.
* Understanding of statistical models and efficacy data analysis.
* Knowledge of global drug development regulations and submission requirements.
Core Competencies
* Strategic and analytical mindset with strong problem‑solving skills.
* Excellent communication and collaboration across global and cross‑functional teams.
* Ability to influence without direct authority.
* High attention to detail and commitment to quality and compliance.
* Proven ability to manage timelines and deliverables in a fast‑paced environment.
London, England, United Kingdom
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