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Associate Director, Statistical Programming
Gilead SciencesAssociate Director leading statistical programming tool development at Gilead. Overseeing multiple studies, ensuring high-quality delivery and compliance with standards.
Posted 7/16/2026full-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.
Demonstrates advanced expertise in statistical programming and tool development, particularly with SAS Macros, while effectively leading projects and teams within the life sciences domain. Strong understanding of clinical trial design, regulatory requirements, and the ability to communicate effectively across functions is essential.
Highest-signal resume keywords
SAS Macro DevelopmentStatistical ProgrammingProject LeadershipClinical Trial DesignRegulatory Reporting
ATS Keywords
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Hard Skills
Statistical ProgrammingTool DevelopmentSAS MacroAutomation SolutionsClinical Trials Analysis
Soft Skills
Excellent CommunicationInterpersonal Skills
Certifications & Qualifications
PhDMSBS
Industry Keywords
Life SciencesClinical TrialsRegulatory RequirementsProject Management
About the role
Key responsibilities & impact- Leads statistical programming tool development (e.g., SAS macros, automation solutions) supporting multiple studies and/or workstreams
- Accountable for planning and delivery of tool development aligned with study and business timelines
- Influences design, development, qualification, and maintenance of SAS macros and related tools
- Acts as a project or functional lead for statistical programming tool initiatives
- Represents Clinical Data Engineering and Macro Support in cross-functional meetings
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
- Excellent verbal and written communication and interpersonal skills
Benefits
Comp & perks- paid time off
- discretionary annual bonus
- discretionary stock-based long-term incentives
- company-sponsored medical, dental, vision, and life insurance plans