Director, Biostatistics – Virology

Gilead Sciences

Director of Biostatistics overseeing Virology drug discovery and development at Gilead. Leading statistical analysis and collaborating with cross-functional teams in clinical trials.

Posted 6/20/2026full-timeFoster City • California, New Jersey • 🇺🇸 United StatesLead💰 $205,615 - $292,710 per yearWebsite

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Hard Skills

statistical leadershiptrial designstatistical data analysisstatistical principlesdrug developmentNDA filingBLA filingbiomedical data analysisSASR

Soft Skills

effective communicationcollaborationinterpersonal skillsteam leadershipstrategic risk assessmentcareer developmentnegotiationrelationship buildingclear directionshared vision

Certifications & Qualifications

PhDMasters degreeBachelors degree

Industry Keywords

Virologyclinical trialsphase 1 trialsphase 2 trialsphase 3 trialsHealth Authority interactionsRegulatory requirementsproject managementstatistical programmingclinical research

About the role

Key responsibilities & impact

Provide Statistical leadership to Virology clinical trials: developing trial design options and providing high quality decision support.
Statistical lead for a specific Virology molecule/indication in Health Authority interactions and maintain an accountability thread to TA head
Works collaboratively with Statistical Programming, Biostatistics, Clinical Research, Clinical Data Management, Global Drug Safety, Regulatory and Project Management management/staff to meet project deliverables and timelines for statistical data analysis and reporting.
Uses knowledge of Regulatory requirements regarding statistical principles to ensure the company meets its Regulatory, scientific, and business objectives.
Collaborates with study investigators, outside experts, and internal colleagues to present and publish trial results and statistical analyses within and outside of the company.
Negotiates project timelines given constraints, works with senior management and Human Resources to identify long-term staffing plans, provides career development opportunities to staff, and participates in strategic risk assessment based on statistical analyses or principles.

Requirements

What you’ll need

PhD with 8+ years of industry experience OR Masters degree with 10+ years of industry experience OR Bachelors degree with 12+ years of industry experience
Extensive hands-on experience in drug development including trial design and analysis of phase 1-3 trials and active participation in NDA/BLA filing through label negotiation
Industry experience in the statistical analysis of biomedical data using statistical software (SAS and R experience preferred)
Effective verbal and written communication skills with the ability to convey complex concepts in clear, concise, and accessible language
Strong collaboration and interpersonal skills with demonstrated success in fostering effective relationships and working seamlessly within diverse cross-functional team
Demonstrated ability to assemble and lead high-performing teams, providing clear direction and fostering a shared vision for success

Benefits

Comp & perks

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