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Clinical Statistical Programmer Jobs in Washington

Bachelor's or Master's degree in Statistics or related field 5+ years of SAS programming experience in clinical research Experience with CDISC standards Preferred Qualifications: Experience ...

... degree in Statistics or related field • 5+ years of SAS programming experience in clinical research • Experience with CDISC standards Preferred Qualifications: • Experience supporting FDA ...

... degree in Statistics or related field • 5+ years of SAS programming experience in clinical research • Experience with CDISC standards Preferred Qualifications: • Experience supporting FDA ...

Minimum of 3-5 years of experience in a CRO environment Demonstrated proficiency with statistical methods and applications in clinical research Strong programming skills in SAS and/or R. Ability to ...

Collaborate with statisticians, epidemiologists, and data analysts to ensure data accuracy and ... Strong understanding of ICD10, ICD10CM, ICD10PCS, and clinical terminology standards. * Experience ...

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Clinical Statistical Programmer information

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$18

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How much do clinical statistical programmer jobs pay per hour?

As of Jun 17, 2026, the average hourly pay for clinical statistical programmer in Washington is $61.36, according to ZipRecruiter salary data. Most workers in this role earn between $38.94 and $92.31 per hour, depending on experience, location, and employer.

What are some common challenges faced by Clinical Statistical Programmers when working with clinical trial data?

Clinical Statistical Programmers often encounter challenges such as handling large and complex datasets, ensuring data integrity, and adhering to strict regulatory guidelines (like CDISC standards). Collaborating closely with biostatisticians, data managers, and clinical teams is essential to resolve data discrepancies and meet tight project deadlines. Staying updated on evolving regulatory requirements and software tools is also vital to maintain high-quality deliverables in a fast-paced environment.

What are the key skills and qualifications needed to thrive as a Clinical Statistical Programmer, and why are they important?

To thrive as a Clinical Statistical Programmer, you need strong proficiency in statistical programming languages (such as SAS or R), a background in statistics or life sciences, and familiarity with clinical trial processes. Experience with CDISC standards (SDTM, ADaM), regulatory submission requirements, and version control systems is highly valued. Attention to detail, problem-solving abilities, and effective communication are crucial soft skills for collaborating with cross-functional teams and ensuring data quality. These skills ensure the accurate analysis and reporting of clinical data, which is critical for regulatory compliance and successful clinical trial outcomes.

What does a Clinical Statistical Programmer do?

A Clinical Statistical Programmer is responsible for managing and analyzing clinical trial data using statistical software, such as SAS or R. Their primary tasks include creating datasets, programming statistical analyses, and generating tables, listings, and figures for clinical study reports. They work closely with biostatisticians and clinical research teams to ensure data accuracy and regulatory compliance. Their work is essential for supporting submissions to regulatory agencies and for making data-driven decisions in clinical research.

What Does a Clinical Statistical Programmer Do?

The job duties of a clinical statistical programmer involve collecting data, performing statistical analysis, and analyzing data sets according to the needs of their employer or client. Your responsibilities in this career may involve using SAS programming to create and analyze data sets during clinical trials or other clinical experiments and studies. You may also be involved in performing data integration for reports following clinical research or statistical analysis for quality control (QC).

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SAS Programmer

SAS Programmer

VENESCO, LLC

Falls Church, VA • On-site, Remote

Other

Posted 9 days ago


Job description

Description

SAS Programmer

Location: Remote/Hybrid
Job Type: Full-Time

Position Overview:
Venesco is seeking a skilled SAS Programmer to support clinical data analysis and regulatory submission activities.


Requirements

Key Responsibilities:   Develop SAS programs for tables, listings, and figures (TLFs)   Create CDISC-compliant datasets (SDTM and ADaM)   Validate and document programming outputs   Collaborate with statisticians and data management teams   Support regulatory submissions and audits

Minimum Qualifications:   Bachelor's or Master's degree in Statistics or related field   5+ years of SAS programming experience in clinical research   Experience with CDISC standards

Preferred Qualifications:   Experience supporting FDA submissions   Knowledge of Python