Senior Principal Statistical Programmer — Lead DMC & SAS (Remote)

WCG Clinical, Inc.; Dover; Remoto; GBP 98.000 - 120.000; Tempo pieno

Vantaggi offerti da questo lavoro

Medical insurance

Dental insurance

Vision insurance

401(k) with company match

Tuition reimbursement

On-the-job training

Continuing education support

Paid holidays

Vacation

Sick time

Descrizione del lavoro

WCG Clinical, Inc. is seeking a Senior Principal Statistical Programmer to lead advanced programming for clinical trials and DMC deliverables. This role blends hands-on SAS/R programming with technical leadership to standardize outputs, mentor staff, and drive best practices across projects.

You will collaborate with biostatistics, data management, and cross-functional teams to ensure compliant, high-quality programming for regulatory submissions and CDISC standards. Remote US-based position.

Competenze

• 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.

Mansioni

• 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 statistical analysis plans (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.

Conoscenze

SAS programming

R programming

Regulatory deliverables

Formazione

Master’s degree

CDISC standards

Descrizione del lavoro

WCG Clinical, Inc. is seeking a Senior Principal Statistical Programmer to lead advanced programming for clinical trials and DMC deliverables. This role blends hands-on SAS/R programming with technical leadership to standardize outputs, mentor staff, and drive best practices across projects.

You will collaborate with biostatistics, data management, and cross-functional teams to ensure compliant, high-quality programming for regulatory submissions and CDISC standards. Remote US-based position.