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# Remote Senior Statistical Programmer/Analyst Consultant Remote at UK (CVRM- Cardiovascular, Renal & Metabo

- **Company:** Clinchoice
- **Location:** Lanark, UK (Remote available)
- **Experience:** Expert
- **Contract:** Permanent contract
- **Skills:** Computer Programming, SAS (Software), Information Technology, Data Management, Intercompany Hub
- **Published:** October 4, 2026
- **Apply:** https://www.apply4u.co.uk/jobs/remote-senior-statistical-programmeranalyst-consultant-remote-at-uk-cvrm-cardiovascular-renal-metabo/50330223

## About the Role

reporting Collaborate with Biostatistics, Data Management, and Clinical teams Ensure programming deliverables meet quality standards and project timelines Participate in study planning, review specifications, and support submission activities Bachelor's degree in computer science (CS), statistics, or related scientific disciplines with 5 yrs. of clinical programming (CDISC) experience; Master's degree in CS, statistics or related disciplines with 6 yrs. of clinical programming (CDISC) experience. Working knowledge of ICH and Good Clinical Practices, Clinical research, Clinical trial process, and related regulatory requirements and terminology. If you have the requirements we need, you will be invited for phone interview as the first step. ClinChoice is a global full-service CRO specializing in clinical development and functional solutions for pharmaceutical, biotechnology, medical device, and consumer health companies. We have over 28 years of proven high-quality delivery and results

## Description

Are you interested in working directly for a single sponsor while having the security and additional career opportunities that working for a global CRO can bring? ClinChoice is a global full-service CRO with a strong focus on quality, professional development, and supportive culture. The Senior Statistical Programmer Consultant is a delivery-focused role who works under the leadership, oversight, and direction of a Programming team leader to lead and/or support aspects of the programming effort to deliver technical programming and information components of a project. This position requires high technical skills and thorough industry knowledge to independently perform the Programming tasks Strong SAS programming experience within the pharmaceutical/CRO industry Hands-on experience supporting CVRM (Cardiovascular, Renal & Metabolism) studies Experience supporting regulatory submissions is preferred Develop, validate, and maintain SAS programs for clinical study data analysis and


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