Senior Manager, Statistical Programming

Gilead Sciences

Senior Manager, Statistical Programming at Gilead creating analysis datasets for regulatory submissions. Leading programming efforts and collaborating with internal and external teams in hybrid work settings.

Posted 7/14/2026full-timeSan Francisco • California, North Carolina • 🇺🇸 United StatesSenior💰 $169,320 - $219,120 per yearWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in statistical data analysis and reporting within clinical development, with a strong foundation in biostatistics and programming for regulatory submissions. Capable of managing complex projects and collaborating across departments to ensure timely and accurate deliverables.

Highest-signal resume keywords

BiostatisticsStatistical Data AnalysisClinical Trials DesignRegulatory Reporting RequirementsProgramming Support

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Statistical AnalysisProgramming DeliverablesData SubmissionAnalysis File DesignDocumentation ComplianceIntegrated Analysis ActivitiesUser-Defined Statistical ReportsComplex Task ManagementResource AnticipationFDA Submission Experience

Soft Skills

Excellent Communication SkillsAnalytical SkillsConflict ResolutionNegotiation SkillsCollaboration

Certifications & Qualifications

BS Degree in Biostatistics/Computer ScienceMS Degree in Biostatistics/Computer SciencePhD Degree in Biostatistics/Computer Science

Industry Keywords

PharmaBiotechFDAPMDAEMATherapeutic AreasElectronic Data SubmissionsStudy ReportsIntegrated SummariesStrategic Initiatives

About the role

Key responsibilities & impact

Work collaboratively with Clinical Development staff to meet project deliverables and timelines for statistical data analysis and reporting
Generate or oversee the production of programming deliverables (e.g., tables, figures, listings) for study reports and integrated summaries
Anticipate resource needs
Direct the design and/or coding of analysis files
Ensure programming and corresponding documentation is completed in a manner that is consistent with departmental procedures
Provide primary and secondary programming support as needed
Implement strategic initiatives

Requirements

What you’ll need

BS degree in Biostatistics/Computer Science or equivalent and 8+ years’ experience in pharma/biotech OR MS degree in Biostatistics/Computer Science or equivalent and 4+ years’ experience in pharma/biotech OR PhD degree in Biostatistics/Computer Sciences or equivalent 2+ years of experience in pharma/biotech
Excellent verbal and written communication skills
Solid analytical skills with advanced knowledge of statistics
Proven track record on multiple, time-sensitive, and complex tasks
Thorough understanding of clinical trials design and reporting processes
Understanding of regulatory reporting requirements including electronic data submissions for multiple therapeutic areas, especially with FDA, PMDA, EMA, etc.
Experience with integrated analysis activities for FDA submissions plus their post-filing activities
Ability to interact with other departments to define and produce user-defined statistical reports
Ability to resolve study related issues and conflicts within a therapeutic project
Ability to create buy-in and support and negotiate timelines

Benefits

Comp & perks

company-sponsored medical, dental, vision, and life insurance plans
discretionary annual bonus
discretionary stock-based long-term incentives (eligibility may vary based on role)
paid time off