Associate Director, Biostatistics – Virology

Gilead Sciences

. Provide strategic and operational statistical input for clinical development programs within the Virology Therapeutic Area .

Posted 10/16/2026full-timeUnited StatesSenior💰 $195,670 - $253,220 per yearWebsite

Core Competencies

Role fit

Core Competencies

Use this summary to align your resume positioning with the role.

Demonstrates expertise in statistical analysis and biostatistics for clinical trials, with a strong focus on Phase 1–3 study design, regulatory compliance, and cross-functional collaboration. Proven leadership in developing talent and fostering inclusive teams within the Virology Therapeutic Area.

Highest-signal resume keywords

Statistical AnalysisBiostatisticsClinical TrialsRegulatory RequirementsAdvanced Statistical Software

ATS Keywords

Tailor your resume

Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills

Statistical AnalysisBiostatisticsStatistical SoftwareStudy DesignSample Size DeterminationStatistical Analysis PlansData Analysis TechniquesClinical Development PlansProtocol DevelopmentStatistical Reporting

Soft Skills

CollaborationLeadershipCommunicationTeam EmpowermentStrategic Thinking

Certifications & Qualifications

PhD Preferred

Industry Keywords

Virology Therapeutic AreaGilead SOPsClinical DevelopmentPatient SafetyRegulatory AffairsProject ManagementClinical Data ManagementStatistical Analysis PrinciplesIndustry Standards

About the role

Key responsibilities & impact

Provide strategic and operational statistical input for clinical development programs within the Virology Therapeutic Area
Serve as lead statistician for Phase 1–3 clinical trials with responsibility for overall statistical strategy and delivery
Represent Biostatistics on study management teams and development teams for multiple studies
Collaborate with cross-functional teams to ensure high-quality statistical planning, analysis, interpretation, and reporting
Provide statistical input into study design, clinical development plans, sample size determination, and protocol development
Author statistical analysis plans and review tables, figures, listings, and clinical study reports
Advise internal and external partners on statistical analysis strategies, measurement reliability, model identifiability, and interpretation and presentation of statistical results
Analyze historical and external data using advanced statistical software, methods, and techniques
Provide biostatistical input into clinical development documentation, scientific publications, presentations, and regulatory documentation
Lead or contribute to non-molecule-based activities, department strategic initiatives, and working groups
Develop talent, create inclusion, and empower teams as a people leader

Requirements

What you’ll need

10+ years of relevant experience with BS/BA, or 8+ years of relevant experience with MS/MA or MBA, or 5+ years of relevant experience with PhD
PhD strongly preferred
Advanced statistical software, methods, and techniques
Knowledge of regulatory requirements of study conduct, statistical analysis principles, industry standards, and Gilead SOPs
Ability to provide statistical input for Phase 1–3 clinical trials
Ability to collaborate with Clinical Development, Patient Safety, Clinical Pharmacology, Regulatory Affairs, Project Management, Programming, and Clinical Data Management
On-site availability 3 days per week
Current Gilead employees and contractors should apply via the Internal Career Opportunities portal in Workday

Benefits

Comp & perks

Discretionary annual bonus eligibility
Discretionary stock-based long-term incentives eligibility
Paid time off
Company-sponsored medical insurance
Company-sponsored dental insurance
Company-sponsored vision insurance
Company-sponsored life insurance
Reasonable accommodation assistance during the application process