Senior Nonclinical Statistician

Responsibilities Lead and provide statistical support (minimal supervision) to preclinical/non-clinical teams on all relevant statistical matters. Provide methodological and statistical input across preclinical/non-clinical studies; ensure accurate design/analysis for decision-making and regulatory compliance. Contribute to experimental design, study setup, data capture, statistical methodology/programming, and data analyses. Produce statistical analyses and documentation (planning/prioritization, application forms, analysis reports, statistical memos/reports) and communicate conclusions to scientists. Accountable for statistical operations: sample size/design of experiment (if applicable), randomization plan suitability/compliance (if applicable), and delivery of statistical methodology and reports. Accountable for statistical scientific content: select methodology, drive risk assessment (if applicable), interpret results, and perform exploratory/ad-hoc analyses. Coordinate with internal/external stakeholders (e.g., compliance, functional planner, project managers, CROs) and support activities such as integrated analyses and dossier preparation (IND/CTD) and publication. Cross-functional collaboration: work with junior statisticians/contingent workers; manage outsourced activities to CROs. Qualifications Master’s in a relevant field with 4 years of Life Science industry experience OR PhD in a relevant field with 1 year. Skills/Tools Technical expertise in statistics, data science, and statistical modeling. Proficiency in R. JMP or other software (e.g., SAS or Phython) is a plus. Soft/Language Good communication; effective English (verbal/written). Teamwork, multi-cultural collaboration, time management, autonomous. Benefits High-quality healthcare; prevention/wellness programs; at least 14 weeks gender-neutral parental leave. #J-18808-Ljbffr