Remote Senior Principal Statistical Programmer Leader

WCG Clinical, Inc.

Bismarck (ND)

Remote

USD 131.000 - 160.000

Vollzeit

Vor 5 Tagen
Sei unter den ersten Bewerbenden

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Benefits dieser Stelle

Health insurance
401(k) matching
Tuition reimbursement
Paid holidays and time off
Education and training

Zusammenfassung

WCG Clinical, Inc. is seeking a Senior Principal Statistical Programmer to lead advanced programming for clinical trials with emphasis on DMC deliverables and regulatory submissions. The role combines hands‑on SAS/R work with technical leadership across multiple studies.

You will mentor staff, help set programming standards, and collaborate with biostatistics and data management teams to ensure high quality, regulatory‑compliant outputs. Remote US work is supported.

Qualifikationen

  • 8–10 years of statistical programming experience in a clinical trial environment.
  • SAS programming expertise with complex analyses and regulatory deliverables.
  • Proficiency in R programming.
  • Experience mentoring staff and driving technical standards or best practices.

Aufgaben

  • Lead complex programming deliverables including analysis datasets, tables, listings, and figures.
  • Design, validate, and oversee programming deliverables and DMC macros and standards.
  • Provide technical oversight for regulatory submissions and inspection readiness.
  • Mentor programming staff and drive best practices across studies.
  • Collaborate with biostatistics and study teams to support complex trial designs and analyses.

Kenntnisse

SAS programming
R programming
Leadership
Mentoring staff
Regulatory deliverables

Ausbildung

Master's degree

Tools

CDISC standards
Regulatory submission tools

Jobbeschreibung

WCG Clinical, Inc. is seeking a Senior Principal Statistical Programmer to lead advanced programming for clinical trials with emphasis on DMC deliverables and regulatory submissions. The role combines hands‑on SAS/R work with technical leadership across multiple studies.

You will mentor staff, help set programming standards, and collaborate with biostatistics and data management teams to ensure high quality, regulatory‑compliant outputs. Remote US work is supported.

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