Remote Senior Principal SAS Programmer

WCG Clinical, Inc.; Jackson (MS); Remote; USD 131,000 - 160,000; Full time

Job summary

WCG Clinical, Inc. is seeking a Senior Principal Statistical Programmer with 8–10 years of clinical trial programming experience. You will lead complex analyses, tables, listings, and figures, and drive standards across DMC and regulatory deliverables.

Proficiency in SAS and R, CDISC compliance, and mentoring of staff are essential. This remote role collaborates with biostatistics and study teams to ensure high-quality outputs.

Qualifications

• Master’s degree required; in limited circumstances an equivalent combination of education and directly relevant professional experience may be considered.
• 8–10 years of statistical programming experience in a clinical trial environment.
• Deep expertise in SAS programming, including complex analyses and regulatory deliverables.
• Proficiency in R programming.
• Demonstrated experience with CDISC standards and regulatory requirements.
• Proven ability to independently lead complex programming efforts across studies.
• Experience mentoring staff and driving technical standards or best practices.

Responsibilities

• Lead complex programming deliverables for analyses, tables, listings, and figures.
• Develop, validate, and oversee DMC macros and programming standards.
• Provide technical oversight to ensure quality, compliance, and consistency across deliverables.
• Mentor programming staff and drive best practices.
• Collaborate with biostatistics and study teams on trial designs and analyses.
• Coordinate programming activities across multiple studies or initiatives.
• Support regulatory submissions and inspection readiness.

Skills

SAS programming

R programming

CDISC standards

Leadership

Mentoring

Biostatistics project coordination

Education

Master’s degree

Tools

SAS environments tools

Job description

WCG Clinical, Inc. is seeking a Senior Principal Statistical Programmer with 8–10 years of clinical trial programming experience. You will lead complex analyses, tables, listings, and figures, and drive standards across DMC and regulatory deliverables.

Proficiency in SAS and R, CDISC compliance, and mentoring of staff are essential. This remote role collaborates with biostatistics and study teams to ensure high-quality outputs.