{"schemaVersion":"jobsearcher.job.v1","id":"d987d9bb9024babc399b443b","url":"https://jobsearcher.com/jobs/d987d9bb9024babc399b443b","canonicalUrl":"https://jobsearcher.com/jobs/d987d9bb9024babc399b443b","title":"Senior Statistical Programmer (Remote)","description":"About WCG\n\nWCG delivers transformational solutions that accelerate clinical research and advance human health. We serve the experts, innovators, and pathfinders on the frontlines of science and medicine—empowering them to develop breakthrough therapies while ensuring the risks of progress never outweigh the value of human life. Together, we stimulate growth, maximize efficiency, and shape the future of clinical trials.\n\nWhy WCG\n\nAt WCG, we invest in our people because you are the driving force behind our mission. When you grow, our impact grows. When you thrive, research accelerates. We empower you to build a meaningful career while advancing the work that improves lives.\n\nWhat we offer:\n\nComprehensive health and financial protection – Medical, dental, vision, life and disability insurance, 401(k) with company match, and flexible spending accounts\nResources that support your whole life – Employee assistance programs and work/life balance tools\nInvestment in your growth – Referral bonuses, tuition reimbursement, on-the-job training, certification assistance, and continuing education support\nTime to recharge – Paid holidays, vacation, and sick time\nPathways forward – Career development opportunities across One WCG\n\nWe practice transparency in everything we do, including compensation. The salary range for this position reflects our commitment to fair, competitive pay based on your qualifications, experience, skills, education, and location. Together, we'll find the right fit for your expertise and our shared mission.\n\nJob Summary\n\nThe 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.\n\nESSENTIAL 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.\n\nDevelop, validate, and document SAS programs for clinical trial datasets (SDTM, ADaM) and outputs (tables, listings, figures) for regulatory submission, ensuring accuracy and compliance.\nLead programming activities and manage resources, timelines, and priorities for assigned studies and projects.\nConduct comprehensive quality control checks and peer code reviews on all programming deliverables.\nCollaborate with statisticians, data managers, and clinical teams to ensure project requirements are met and deliverables are aligned.\nConduct thorough quality control checks on programs and datasets to ensure precision and dependability.\nOversee and manage programming activities for studies or projects, handling resource allocation, timelines, and budgets.\nGuide junior programmers, offering mentorship on industry standards and best practices.\nProvide expertise in interpreting and implementing Statistical Analysis Plan (SAP) programming specifications and project documentation.\nTroubleshoot programming and data issues, resolve discrepancies, and ensure timely, reliable data reporting.\nCoordinate multiple projects concurrently, setting strategic goals and adapting to evolving priorities.\nFoster innovation within the department and contribute to process enhancement initiatives\nOther duties as assigned by supervisor. These may, on occasion, be unrelated to the position described here.\n\nEDUCATION REQUIREMENTS: Master’s degree in Statistics, Computer Science, Mathematics, Life Sciences, or a related field required.\n\nCERTIFICATIONS/LICENSE/REGISTRATION REQUIREMENTS: SAS Certification preferred.\n\n QUALIFICATIONS/EXPERIENCE:\n\nAt least 5 years of SAS programming experience required.\nR programming experience highly preferred.\n2 years of macro programming experience required.\nAt least 3 years of experience in the pharmaceutical, vaccines, biotech, or medical device industry required.\nPhase 1- 4 clinical trials experience.\nIn depth knowledge of CDISC requirements required.\nUnderstanding of Statistical Analysis Plan programming specifications.\nAttention to detail, accuracy, initiative, and excellent communication skills are essential, as well as the ability to juggle several complex tasks simultaneously.\n\nTRAVEL REQUIREMENTS:\n\n 0% – 5%\n\n 5% - 10%\n\n 10% - 20%\n\n 20% - 50%\n\n >50%\n\nPhysical and Sensory Requirements: The physical and sensory requirements described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be offered to individuals with disabilities to assist in performing the essential functions of the position. Work activities involve light to moderate physical effort (for example, sitting in one place for extended periods of time, standing, walking, bending, lifting lightweight objects, intermittent to sustained periods of keyboarding). Majority of time is spent in a seated position with frequent opportunity to move about at will. Activities require a variety of easy muscle movements. Work activities involve a frequent need to concentrate on a variety of sensory inputs for moderate to lengthy durations at a time requiring diligence and attention to interpret effectively. There will be a need to attend to single or simultaneous tasks where accuracy of details is important. The need for detailed and precise work is high.\n\n#LI-Remote\n\nPay Range\nUSD $104,750.00 - USD $128,000.00 /Yr.\nEEOC Statement\n\nWCG is proud to be an equal opportunity employer. Qualified applicants will receive consideration for employment based on merit and without regard to race, color, national origin or ancestry, religion or creed, sex, sexual orientation, gender expression, gender identity, age, marital status, family or parental status, disability, genetic information, citizenship, veteran status, or any other legally recognized basis or status protected by federal, state, or local law. WCG complies with the Vietnam Era Veterans' Readjustment Act and Section 503 of the Rehabilitation Act. We promote a \"One WCG\" culture where all are welcome, respected, valued, and empowered to make a difference every day to advance clinical research.","company":"Wcg Irb","rawCompany":"wcg irb","isRemote":true,"isActive":false,"createdAt":"2026-09-04T10:32:56.954Z","occupations":[{"code":"15-2041.00","title":"Statisticians","slug":"statisticians"},{"code":"15-2041.01","title":"Biostatisticians","slug":"biostatisticians"},{"code":"43-9111.00","title":"Statistical Assistants","slug":"statistical-assistants"}],"industries":[{"code":"541690","title":"Other Scientific and Technical Consulting Services","slug":"other-scientific-and-technical-consulting-services"},{"code":"541714","title":"Research and Development in Biotechnology (except Nanobiotechnology)","slug":"research-and-development-in-biotechnology-except-nanobiotechnology"},{"code":"541715","title":"Research and Development in the Physical, Engineering, and Life Sciences (except Nanotechnology and Biotechnology)","slug":"research-and-development-in-the-physical-engineering-and-life-sciences-except-nanotechnology-and-biotechnology"}],"jobPosting":{"@context":"https://schema.org","@type":"JobPosting","title":"Senior Statistical Programmer (Remote)","description":"About WCG\n\nWCG delivers transformational solutions that accelerate clinical research and advance human health. We serve the experts, innovators, and pathfinders on the frontlines of science and medicine—empowering them to develop breakthrough therapies while ensuring the risks of progress never outweigh the value of human life. Together, we stimulate growth, maximize efficiency, and shape the future of clinical trials.\n\nWhy WCG\n\nAt WCG, we invest in our people because you are the driving force behind our mission. When you grow, our impact grows. When you thrive, research accelerates. We empower you to build a meaningful career while advancing the work that improves lives.\n\nWhat we offer:\n\nComprehensive health and financial protection – Medical, dental, vision, life and disability insurance, 401(k) with company match, and flexible spending accounts\nResources that support your whole life – Employee assistance programs and work/life balance tools\nInvestment in your growth – Referral bonuses, tuition reimbursement, on-the-job training, certification assistance, and continuing education support\nTime to recharge – Paid holidays, vacation, and sick time\nPathways forward – Career development opportunities across One WCG\n\nWe practice transparency in everything we do, including compensation. The salary range for this position reflects our commitment to fair, competitive pay based on your qualifications, experience, skills, education, and location. Together, we'll find the right fit for your expertise and our shared mission.\n\nJob Summary\n\nThe 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.\n\nESSENTIAL 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.\n\nDevelop, validate, and document SAS programs for clinical trial datasets (SDTM, ADaM) and outputs (tables, listings, figures) for regulatory submission, ensuring accuracy and compliance.\nLead programming activities and manage resources, timelines, and priorities for assigned studies and projects.\nConduct comprehensive quality control checks and peer code reviews on all programming deliverables.\nCollaborate with statisticians, data managers, and clinical teams to ensure project requirements are met and deliverables are aligned.\nConduct thorough quality control checks on programs and datasets to ensure precision and dependability.\nOversee and manage programming activities for studies or projects, handling resource allocation, timelines, and budgets.\nGuide junior programmers, offering mentorship on industry standards and best practices.\nProvide expertise in interpreting and implementing Statistical Analysis Plan (SAP) programming specifications and project documentation.\nTroubleshoot programming and data issues, resolve discrepancies, and ensure timely, reliable data reporting.\nCoordinate multiple projects concurrently, setting strategic goals and adapting to evolving priorities.\nFoster innovation within the department and contribute to process enhancement initiatives\nOther duties as assigned by supervisor. These may, on occasion, be unrelated to the position described here.\n\nEDUCATION REQUIREMENTS: Master’s degree in Statistics, Computer Science, Mathematics, Life Sciences, or a related field required.\n\nCERTIFICATIONS/LICENSE/REGISTRATION REQUIREMENTS: SAS Certification preferred.\n\n QUALIFICATIONS/EXPERIENCE:\n\nAt least 5 years of SAS programming experience required.\nR programming experience highly preferred.\n2 years of macro programming experience required.\nAt least 3 years of experience in the pharmaceutical, vaccines, biotech, or medical device industry required.\nPhase 1- 4 clinical trials experience.\nIn depth knowledge of CDISC requirements required.\nUnderstanding of Statistical Analysis Plan programming specifications.\nAttention to detail, accuracy, initiative, and excellent communication skills are essential, as well as the ability to juggle several complex tasks simultaneously.\n\nTRAVEL REQUIREMENTS:\n\n 0% – 5%\n\n 5% - 10%\n\n 10% - 20%\n\n 20% - 50%\n\n >50%\n\nPhysical and Sensory Requirements: The physical and sensory requirements described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be offered to individuals with disabilities to assist in performing the essential functions of the position. Work activities involve light to moderate physical effort (for example, sitting in one place for extended periods of time, standing, walking, bending, lifting lightweight objects, intermittent to sustained periods of keyboarding). Majority of time is spent in a seated position with frequent opportunity to move about at will. Activities require a variety of easy muscle movements. Work activities involve a frequent need to concentrate on a variety of sensory inputs for moderate to lengthy durations at a time requiring diligence and attention to interpret effectively. There will be a need to attend to single or simultaneous tasks where accuracy of details is important. The need for detailed and precise work is high.\n\n#LI-Remote\n\nPay Range\nUSD $104,750.00 - USD $128,000.00 /Yr.\nEEOC Statement\n\nWCG is proud to be an equal opportunity employer. Qualified applicants will receive consideration for employment based on merit and without regard to race, color, national origin or ancestry, religion or creed, sex, sexual orientation, gender expression, gender identity, age, marital status, family or parental status, disability, genetic information, citizenship, veteran status, or any other legally recognized basis or status protected by federal, state, or local law. WCG complies with the Vietnam Era Veterans' Readjustment Act and Section 503 of the Rehabilitation Act. We promote a \"One WCG\" culture where all are welcome, respected, valued, and empowered to make a difference every day to advance clinical research.","datePosted":"2026-09-04T10:32:56.954Z","dateModified":"2026-09-04T10:32:56.954Z","hiringOrganization":{"@type":"Organization","name":"Wcg Irb","sameAs":"https://jobsearcher.com"},"jobLocationType":"TELECOMMUTE","applicantLocationRequirements":{"@type":"Country","name":"US"},"identifier":{"@type":"PropertyValue","name":"JobSearcher","value":"d987d9bb9024babc399b443b"},"url":"https://jobsearcher.com/jobs/d987d9bb9024babc399b443b"}}