Senior Principal Statistical Programmer — Remote

WCG Clinical; Santa Fe (NM); Remote; USD 131.000 - 160.000; Vollzeit

Benefits dieser Stelle

Health insurance

401(k) with company match

Tuition reimbursement

Zusammenfassung

WCG is seeking a Senior Principal Statistical Programmer to lead complex programming for clinical trials, deliver SAS and CDISC-based outputs, and guide standards and mentoring across projects. You will partner with biostatistics, data management, and IT to ensure compliant, scalable results.

The role emphasizes advanced programming, technical leadership, and alignment with regulatory submissions and DMC deliverables.

Qualifikationen

• Minimum 8–10 years of statistical programming experience in a clinical trial environment.
• Deep expertise in SAS programming, including regulatory deliverables.
• Proficiency in R programming.
• Experience with CDISC standards and regulatory requirements.
• Proven ability to lead complex programming efforts across studies.
• Experience mentoring staff and driving technical standards.

Aufgaben

• Serve as a senior technical expert in statistical programming across multiple studies.
• Design, develop, validate, and oversee complex programming deliverables.
• Lead development and standards for DMC macros and programming.
• Provide technical oversight to ensure quality and regulatory compliance.
• Drive programming standards and process improvements.
• Collaborate with biostatistics and study teams on designs and analyses.
• Independently manage programming activities across initiatives.
• Mentor programming staff and share best practices.
• Contribute to proposals, planning, and scope discussions.
• Partner with IT to support SAS environments and system validation.
• Ensure deliverables meet submission requirements and CDISC.
• Influence approaches and practices across programs.

Kenntnisse

SAS programming

R programming

CDISC

Leadership

Mentoring

Project coordination

Ausbildung

Master’s degree

Jobbeschreibung

WCG is seeking a Senior Principal Statistical Programmer to lead complex programming for clinical trials, deliver SAS and CDISC-based outputs, and guide standards and mentoring across projects. You will partner with biostatistics, data management, and IT to ensure compliant, scalable results.

The role emphasizes advanced programming, technical leadership, and alignment with regulatory submissions and DMC deliverables.