Senior Statistical Programmer/Analyst Consultant – CVRM, Cardiovascular, Renal & Metabolism

ClinChoice

Senior Statistical Programmer Consultant at ClinChoice involved in technical programming for clinical studies, delivering high-quality programming tasks with a focus on CVRM.

Posted 5/19/2026contractRemote • 🇬🇧 United KingdomSeniorWebsite

About the role

Key responsibilities & impact

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.
Develop, validate, and maintain SAS programs for clinical study data analysis and reporting.
Create datasets, tables, listings, and figures according to study requirements.
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.

Requirements

What you’ll need

Strong SAS programming experience within the pharmaceutical/CRO industry
Hands-on experience supporting CVRM (Cardiovascular, Renal & Metabolism) studies
Experience in generating and validating SDTM, ADaM, and TLFs
Good understanding of CDISC standards and clinical trial processes
Ability to work independently and manage multiple priorities in a fast-paced environment
Experience supporting regulatory submissions is preferred
Strong communication and stakeholder management skills.

Benefits

Comp & perks

ClinChoice offers a strong focus on quality, professional development, and supportive culture.

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills & Tools

SAS programmingSDTMADaMTLFsdata analysisdata validationdataset creationclinical study reportingprogramming deliverablesregulatory submissions

Soft Skills

communicationstakeholder managementindependent workpriority managementcollaboration