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# Statistical Programmer/Analyst Consultant (Cardiovascular, Renal)

- **Company:** ClinChoice Inc
- **Location:** New York, NY, United States (Remote available)
- **Experience:** Expert
- **Contract:** Permanent contract
- **Skills:** Computer Programming, SAS (Software), Information Technology, Data Management, Intercompany Hub
- **Published:** August 9, 2026
- **Apply:** https://www.workingnomads.com/job/go/1780793/

## About the 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. This position requires high technical skills and thorough industry knowledge to independently perform the Programming tasks

Key Requirement:

 * 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, * 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.
 * Need to have Respiratory/Immunology TA experience.
 * Working knowledge of ICH and Good Clinical Practices, Clinical research, Clinical trial process, and related regulatory requirements and terminology.

## Description

* 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


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