Senior Manager, Statistical Programming

Gilead Sciences

Senior Manager, Statistical Programming at Gilead overseeing statistical datasets and reports. Collaborating with teams to ensure timely analysis and delivery for regulatory submissions.

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 programming within the pharmaceutical and biotech industries, with a strong focus on clinical trial design, regulatory reporting, and effective communication across departments.

Highest-signal resume keywords

BiostatisticsStatistical Data AnalysisClinical Trials DesignRegulatory ReportingProgramming Support

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Statistical AnalysisProgramming DeliverablesData DocumentationAnalysis File DesignUser-Defined Statistical Reports

Soft Skills

Excellent Communication SkillsInterpersonal SkillsAnalytical SkillsConflict ResolutionNegotiation Skills

Industry Keywords

PharmaBiotechFDAPMDAEMAElectronic Data SubmissionsIntegrated Analysis ActivitiesTherapeutic Areas

About the role

Key responsibilities & impact

Works collaboratively with Clinical Development staff to meet project deliverables and timelines for statistical data analysis and reporting.
Generates or oversees the production of programming deliverables (e.g., tables, figures, listings) for study reports and integrated summaries.
Anticipates resource needs
Directs the design and/or coding of analysis files.
Ensures programming and corresponding documentation is completed in a manner that is consistent with departmental procedures.
Provides primary and secondary programming support as needed.
Implements 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 and interpersonal skills are required.
Solid analytical skills with advanced knowledge of statistics
Proven track record on multiple, time-sensitive, and complex tasks
Has a thorough understanding of clinical trials design and reporting processes, as well as regulatory reporting requirements including electronic data submissions for multiple therapeutic areas, especially with FDA, PMDA, EMA, and other global agencies.
Experience with integrated analysis activities for FDA and rest of world submissions plus their post-filing activities.
Must be able to interact with other departments to define and produce user-defined statistical reports (e.g., ad hoc requests).
Has the ability to resolve study related issues and conflicts within a therapeutic project.
Can create buy-in and support and can 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