Senior SAS Programmer: Lead Clinical Data & Submissions

WCG Clinical, Inc.; Carson City (NV); Remote; USD 105,000 - 128,000; Full time

Job summary

WCG seeks a Senior Statistical Programmer to develop, validate, and document SAS programs for clinical trial data analyses and regulatory submissions. You will lead programming activities, ensure quality and regulatory compliance, and mentor junior staff.

You will collaborate with statisticians, data managers, and clinical teams to meet study requirements, troubleshoot data issues, and drive process improvements in a US-Remote setting.

Qualifications

• Master's degree in Statistics, Computer Science, Mathematics, Life Sciences, or a related field required.
• At least 5 years of SAS programming experience required.
• R programming experience highly preferred.
• 2 years of macro programming experience required.
• At least 3 years of experience in the pharmaceutical, vaccines, biotech, or medical device industry required.
• Phase 1-4 clinical trials experience.
• In depth knowledge of CDISC requirements required.

Responsibilities

• Develop, validate, and document SAS programs for clinical trial datasets (SDTM, ADaM) and outputs (tables, listings, figures) for regulatory submission, ensuring accuracy and compliance.
• Lead programming activities and manage resources, timelines, and priorities for assigned studies and projects.
• Conduct comprehensive quality control checks and peer code reviews on all programming deliverables.
• Collaborate with statisticians, data managers, and clinical teams to ensure project requirements are met and deliverables are aligned.
• Troubleshoot programming and data issues, resolve discrepancies, and ensure timely, reliable data reporting.
• Oversee and manage programming activities for studies or projects, handling resource allocation, timelines, and budgets.
• Guide junior programmers, offering mentorship on industry standards and best practices.

Skills

SAS programming

R programming

Macro programming

CDISC

SAP programming specifications

Education

Master's degree in Statistics/CS/Math/Life Sciences

Job description

WCG seeks a Senior Statistical Programmer to develop, validate, and document SAS programs for clinical trial data analyses and regulatory submissions. You will lead programming activities, ensure quality and regulatory compliance, and mentor junior staff.

You will collaborate with statisticians, data managers, and clinical teams to meet study requirements, troubleshoot data issues, and drive process improvements in a US-Remote setting.