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Agent guide: [/agents.md](https://www.wearedevelopers.com/agents.md). --- # Senior Statistical Programmer (Remote) - **Company:** WCG Clinical - **Location:** Cary, NC, United States (Remote available) - **Experience:** Expert - **Salary:** $128,000.0 - **Contract:** Permanent contract - **Skills:** Computer Programming, R (Programming Language), SAP (Applications), SAS (Software), Information Technology - **Published:** September 4, 2026 - **Apply:** https://www.techcareers.com/job.asp?id=3377270631&tx=KP4545FFL&pt=1&aff=0B19D771-A501-4A5E-8338-2A822B784D54&utm_source=Job%20Feed&utm_medium=textkernel&utm_campaign=DE&utm_term=0B19D771-A501-4A5E-8338-2A822B784D54 ## About the Role EDUCATION REQUIREMENTS: Master's degree in Statistics, Computer Science, Mathematics, Life Sciences, or a related field required. CERTIFICATIONS/LICENSE/REGISTRATION REQUIREMENTS: SAS Certification preferred., * 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. * Understanding of Statistical Analysis Plan programming specifications. * Attention to detail, accuracy, initiative, and excellent communication skills are essential, as well as the ability to juggle several complex tasks simultaneously. TRAVEL REQUIREMENTS: ? 0% - 5% ? 5% - 10% ? 10% - 20% ? 20% - 50% ? >50% ## Description The Senior Statistical Programmer develops, validates, and documents SAS programs to support clinical trial data analysis and regulatory submissions. This role leads programming activities, ensures deliverables meet industry and regulatory standards, and mentors junior programmers. The Senior Statistical Programmer collaborates closely with cross-functional teams, troubleshoots data and programming issues, and advances process improvements to optimize project outcomes. ESSENTIAL DUTIES/RESPONSIBILITIES: To perform this job successfully, an individual must be able to perform each essential duty and responsibility satisfactorily. The accountabilities listed below are representative of the knowledge, skills, and/or ability required. * 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. * Conduct thorough quality control checks on programs and datasets to ensure precision and dependability. * 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. * Provide expertise in interpreting and implementing Statistical Analysis Plan (SAP) programming specifications and project documentation. * Troubleshoot programming and data issues, resolve discrepancies, and ensure timely, reliable data reporting. * Coordinate multiple projects concurrently, setting strategic goals and adapting to evolving priorities. * Foster innovation within the department and contribute to process enhancement initiatives * Other duties as assigned by supervisor. 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