Senior Principal Statistical Programmer - DMC Lead

WiTH Collective

Cary (NC)

Hybrid

USD 104,750 - 128,000

Full time

14 days+

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Benefits offered by this job

Health insurance
Dental insurance
Vision insurance
Life and disability insurance
401k with match
Flexible spending accounts
Employee assistance programs
Work/life resources
Referral bonuses
Tuition reimbursement
Flexible PTO
Volunteer time off
Career development & continuing ed

Job summary

WCG is seeking a Senior Principal Statistical Programmer to lead complex programming initiatives in clinical trials and DMC deliverables. The role combines hands-on coding with technical leadership, shaping standards, tools, and best practices across projects.

You will collaborate with biostatistics, data management, and cross-functional teams to ensure compliant, high-quality outputs and efficient delivery. Master’s degree and 8–10 years’ experience required.

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 independently coordinate biostatistical projects, including planning and oversight of programming activities, with minimal direction from senior leadership.

Responsibilities

  • Serve as a senior technical expert in statistical programming, providing guidance across multiple studies or functional areas.
  • Design, develop, validate, and oversee complex statistical programming deliverables, including analysis datasets, tables, listings, and figures.
  • Lead the development, validation, and continuous improvement of DMC macros and programming standards.
  • Provide technical oversight and review of programming work to ensure quality, compliance, and consistency across deliverables.
  • Drive the establishment and adoption of programming standards, best practices, and process improvements.
  • Collaborate with biostatistics and study teams to support complex trial designs, analyses, and DMC reporting.
  • Independently manage and prioritize programming activities across multiple studies or initiatives.
  • Mentor and provide technical leadership to statistical programming staff, supporting skill development and best practices.
  • Contribute technical expertise to proposals, project planning, and scope discussions as needed.
  • Partner with IT and technology teams to support SAS environments, tools, and system validation efforts.
  • Provide technical oversight for programming activities supporting regulatory submissions and inspection readiness.
  • Ensure programming deliverables align with regulatory expectations, submission requirements, and CDISC standards.
  • Influence programming approaches, standards, and best practices across multiple studies or programs.
  • Serve as a technical escalation point for complex programming, data, or deliverable issues, leading resolution of highly complex or ambiguous challenges.
  • Provide expert interpretation of SAPs, protocols, and study documents, translating requirements into programming strategy.
  • Champion process improvements, automation, and innovative approaches to enhance efficiency, scalability, and consistency of programming deliverables.
  • Other duties as assigned by supervisor.

Skills

SAS programming
R programming
CDISC standards
Leadership
Mentoring
Biostatistics coordination

Education

Master’s degree

Job description

WCG is seeking a Senior Principal Statistical Programmer to lead complex programming initiatives in clinical trials and DMC deliverables. The role combines hands-on coding with technical leadership, shaping standards, tools, and best practices across projects.

You will collaborate with biostatistics, data management, and cross-functional teams to ensure compliant, high-quality outputs and efficient delivery. Master’s degree and 8–10 years’ experience required.

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