Sr Principal Statistical Programmer – Remote SAS/CDISC

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

Benefits offered by this job

Health and financial protection

Work-life balance tools

Tuition reimbursement & continuing Ed

Job summary

WCG Clinical, Inc. seeks a Senior Principal Statistical Programmer to lead complex programming efforts for clinical trials. You will design, validate, and standardize outputs (datasets, tables, listings, figures) and guide macro development for DMC and regulatory deliverables.

You will provide expert oversight across studies, mentor staff, and collaborate with biostatistics and project teams to ensure high quality, compliant results aligned with CDISC standards.

Qualifications

• Minimum 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 is a must.
• 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.
• Demonstrated ability to coordinate biostatistical projects with minimal direction.

Responsibilities

• Serve as a senior technical expert in statistical programming across multiple studies.
• Design, develop, validate, and oversee complex programming deliverables (datasets, tables, listings, figures).
• Lead development, validation, and improvement of DMC macros and programming standards.
• Provide technical oversight to ensure quality, compliance, and consistency.
• Drive programming standards, best practices, and process improvements.
• Collaborate with biostatistics and study teams for complex trial designs and reporting.

Skills

SAS programming

R programming

CDISC standards

Leadership/mentoring

Regulatory deliverables

Education

Master's degree

Tools

SAS

R

Job description

WCG Clinical, Inc. seeks a Senior Principal Statistical Programmer to lead complex programming efforts for clinical trials. You will design, validate, and standardize outputs (datasets, tables, listings, figures) and guide macro development for DMC and regulatory deliverables.

You will provide expert oversight across studies, mentor staff, and collaborate with biostatistics and project teams to ensure high quality, compliant results aligned with CDISC standards.