Senior Statistical Programmer (Remote)

About the role

WCG delivers transformational solutions that accelerate clinical research and advance human health. We empower experts, innovators, and pathfinders on the frontlines of science and medicine 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.

At 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.

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.
• 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.

Requirements

• Master’s degree in Statistics, Computer Science, Mathematics, Life Sciences, or a related field required.
• At least 5 years of SAS programming experience required.
• 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.

Preferred Qualifications

• SAS Certification preferred.
• R programming experience highly preferred.

Benefits

• Comprehensive health and financial protection: medical, dental, vision, life and disability insurance, 401(k) with company match, and flexible spending accounts.
• Resources that support your whole life: employee assistance programs and work/life balance tools.
• Investment in your growth: referral bonuses, tuition reimbursement, on-the-job training, certification assistance, and continuing education support.
• Time to recharge: paid holidays, vacation, and sick time.
• Pathways forward: career development opportunities across One WCG.

Pay

USD $104,750.00 – USD $128,000.00 per year.