Job Description
This position is listed on behalf of a partner company, who manages all applications and next steps. Our partner is looking for a Statistical Programmer based in the United States.
This role sits at the core of clinical research programming, transforming clinical trial data into high-quality statistical outputs that support regulatory submissions, publications, and evidence generation for medical products and devices. You will be responsible for developing, validating, and maintaining robust SAS programs that produce datasets, tables, listings, and figures aligned with Statistical Analysis Plans. The position requires close collaboration with statisticians, data managers, clinical teams, and external vendors to ensure accuracy, consistency, and traceability of all deliverables. You will contribute to the implementation of CDISC standards and support SDTM and ADaM dataset creation in a regulated environment. This is a detail-oriented, impact-driven role where quality, compliance, and scientific rigor are essential. You will also participate in process improvements and modernization efforts that enhance programming efficiency and standardization across studies.
This position is listed on behalf of a partner company, who manages all applications and next steps. Our partner is looking for a Statistical Programmer based in the United States.
This role sits at the core of clinical research programming, transforming clinical trial data into high-quality statistical outputs that support regulatory submissions, publications, and evidence generation for medical products and devices. You will be responsible for developing, validating, and maintaining robust SAS programs that produce datasets, tables, listings, and figures aligned with Statistical Analysis Plans. The position requires close collaboration with statisticians, data managers, clinical teams, and external vendors to ensure accuracy, consistency, and traceability of all deliverables. You will contribute to the implementation of CDISC standards and support SDTM and ADaM dataset creation in a regulated environment. This is a detail-oriented, impact-driven role where quality, compliance, and scientific rigor are essential. You will also participate in process improvements and modernization efforts that enhance programming efficiency and standardization across studies.
