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Associate Director, Statistical Programming
Gilead SciencesAssociate Director leading statistical programming tool development at Gilead. Responsible for delivering high-quality, scalable tools aligned with Clinical Data Science standards.
Posted 7/17/2026full-timeCalifornia, North Carolina • 🇺🇸 United StatesLead💰 $177,905 - $253,220 per yearWebsite
Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Expertise in statistical programming and tool development, particularly with SAS Macros, combined with a strong understanding of clinical trial design and regulatory requirements. Proven ability to lead projects and teams while ensuring high-quality deliverables aligned with business timelines.
Highest-signal resume keywords
SAS Macro DevelopmentStatistical ProgrammingClinical Trial DesignProject LeadershipRegulatory Reporting
ATS Keywords
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Hard Skills
Statistical ProgrammingTool DevelopmentSAS MacroData StandardsStatistical Programming Good Practices
Soft Skills
Project LeadershipInfluencingCollaboration
Certifications & Qualifications
PhDMSBS
Industry Keywords
Life SciencesClinical TrialsRegulatory RequirementsAnalysisStandardized Programming Tools
About the role
Key responsibilities & impact- Leads statistical programming tool development supporting multiple studies and ensuring delivery of high-quality, scalable tools
- Accountable for planning and delivery of tool development aligned with study and business timelines
- Influences design, development, qualification, and maintenance of SAS macros
- Maintains advanced knowledge of statistical programming good practices, data standards and norms
- Drives adoption of standardized programming tools, templates, and methodologies
Requirements
What you’ll need- PhD with 5+ years OR MS with 8+ years, OR BS with 10+ years of relevant experience in statistical programming or related field
- Significant experience in life sciences, including clinical trials, analysis, and regulatory reporting
- Demonstrated experience leading projects and/or teams
- Advanced expertise in statistical programming and tool development (SAS Macro required)
- Strong understanding of clinical trial design and reporting process, as well as regulatory requirements
Benefits
Comp & perks- Health insurance
- Discretionary annual bonus
- Discretionary stock-based long-term incentives
- Paid time off
- Company-sponsored medical, dental, vision, and life insurance plans