Lead the statistical design and analytical planning for oncology clinical utility studies.
Serve as study statistician for multiple studies and collaborate with clinical, medical, and translational partners.
Author and review high-quality statistical deliverables, including statistical analysis plans (SAPs), and reports (TLFs, CSRs, publications).
Recommend and apply novel statistical approaches where appropriate; mentor early career statisticians.

Requirements

Advanced degree in Biostatistics, Statistics, or a related quantitative field (Ph.D. preferred).
4+ years of experience in clinical trial biostatistics.
Strong expertise in time-to-event analysis, including handling of censoring, competing risks, and advanced survival modeling approaches commonly used in oncology.
Expertise with innovative study design (e.g. adaptive and biomarker-informed designs), power calculations, and endpoint evaluation.
Working knowledge of ICH and GCP guidelines as well as CDISC standards (e.g. SDTM, ADaM).
Proficient in R.

Benefits

Comprehensive medical, dental, vision, life and disability plans for eligible employees and their dependents.
Free testing for employees and their immediate families.
Fertility care benefits.
Pregnancy and baby bonding leave.
401k benefits.
Commuter benefits.
Generous employee referral program.

Applicant Tracking System Keywords

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

Hard Skills & Tools

biostatisticsclinical trial biostatisticstime-to-event analysissurvival modelingadaptive study designbiomarker-informed designpower calculationsendpoint evaluationstatistical analysis plansR

Soft Skills

leadershipmentoringcollaborationcommunication

Certifications

Ph.D. in BiostatisticsPh.D. in Statistics