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1–2 jobs· newest first

Principal Biostatistician - Safety (FSP)
Thermo Fisher Scientific · Remote, Belgium
Remote · Senior
Biostatistics Director
Neurocrine Biosciences · Allschwil, Switzerland
Senior

+10K new in the last hour

Principal Biostatistician - Safety (FSP)

Thermo Fisher Scientific · Posted Nov 5, 2026

Remote, Belgium
Remote
Senior
6+ years

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Lead biostatistical analysis for global clinical trials in a biotechnology setting, overseeing study design, protocol writing, analysis, and reporting.

Responsibilities

Implement diverse statistical tasks throughout the full clinical trial process
Develop and review statistical analysis plans
Conduct benefit-risk analysis and safety reporting (DSUR, PSUR)
Manage multiple clinical trials simultaneously
Apply CDISC standards and statistical software (SAS, R, EAST, WinBUGS)

Requirements

Advanced Degree in Statistics, Biostatistics, or related quantitative field
Nice to have: Experience in CRO environment
Nice to have: Vendor management
Nice to have: Auto-immune and/or oncology therapeutic areas

Skills

SAS programming Statistical methodology ICH-GCP guidelines Statistical analysis plan development Benefit-risk analysis Safety reporting CDISC standards R EAST WinBUGS SAS

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Biostatistics Director

Neurocrine Biosciences · Posted May 20, 2026

Allschwil, Basel-Landschaft, Switzerland
Senior
7+ years

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Lead statistical strategy and execution for real‑world evidence studies in a biopharmaceutical setting.

Responsibilities

Develop strategic and operating plans for the area of responsibility
Serve as overall statistical lead and point of contact for Biometrics
Provide strategic and tactical support for cross‑functional RWE development
Serve as subject matter expert for RWE/HEOR research design and methodology
Leverage administrative claims, electronic medical records, or other real‑world data

Requirements

Master’s degree in statistics, biostatistics or related discipline
PhD in statistics, biostatistics or related discipline

Skills

SAS R statistical models machine learning models real‑world evidence (RWE)observational research protocol development

statistical analysis plan development

study report development

regulatory and HTA requirements

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