Contract Opportunity – Senior / Principal Statistical Programmer (UK/EU)
Location: UK or Europe (Remote)
Contract Length: 12 Months (initial contract)
Start Date: ASAP / Flexible for the right person
Rate: Competitive
We're supporting a leading organisation within the pharmaceutical/biotech sector in the search for a Senior / Principal Statistical Programmer to join on a contract basis. This role will play a key part in delivering high-quality programming across clinical development programmes for a US-based client.
Role Overview
* Take ownership of statistical programming deliverables across assigned studies
* Build and validate ADaM and SDTM datasets in accordance with CDISC standards
* Generate tables, listings, and figures to support study outputs and submissions
* Ensure all outputs are submission-ready for regulatory authorities (e.g. FDA, EMA)
* Partner with cross-functional teams including Biostatistics and Data Management
* Support continuous improvement of programming processes and standards
Candidate Profile
* Strong background of SAS programming within Pharma, Biotech, or CRO environments
* Proven experience supporting clinical trials reporting and regulatory submissions
* Strong expertise in CDISC standards (SDTM, ADaM, Define.xml)
* Advanced SAS skills including Macros, SQL, STAT, and GRAPH
* Experience developing technical specifications and complex, validated programs
* Solid understanding of statistical methods applied in clinical research
* Exposure to R programming (preferred)
* Degree in a relevant field (Bachelor's required, Master's preferred)
* Strong communication and organisational skills, with fluent English (essential)
* Able to work remotely with flexibility to align to EU working hours
This is a great opportunity to contribute to impactful clinical research within a flexible and collaborative environment at a leading organisation.
Apply now!