Lead the statistical design and analytical planning for oncology clinical utility studies. Provide
Serve as study statistician for multiple studies. Collaborate with clinical, medical, and
Author and review high-quality statistical deliverables, including statistical analysis plans
Recommend and apply novel statistical approaches where appropriate. Mentor early career

🎯 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
Expertise with innovative study design (e.g. adaptive and biomarker-informed designs), power
Working knowledge of ICH and GCP guidelines as well as CDISC standards (e.g. SDTM, ADaM).
Proficient in R.

🎁 Benefits

Competitive Benefits - Employee benefits include comprehensive medical, dental, vision, life and

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