Senior Statistical Programmer (Remote)

About WCG

WCG 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. 

Why WCG

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. 

What we offer: 

• 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 

We 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. 

Job Summary

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. These may, on occasion, be unrelated to the position described here.

EDUCATION REQUIREMENTS: Master’s degree in Statistics, Computer Science, Mathematics, Life Sciences, or a related field required.

CERTIFICATIONS/LICENSE/REGISTRATION REQUIREMENTS: SAS Certification preferred.  

 QUALIFICATIONS/EXPERIENCE:

• 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%

#LI-Remote

Pay Range

EEOC Statement

WCG 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, pregnancy, 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.