About this role

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.

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.

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

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

Key skills