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Principal Biostatistician - Safety (FSP)
Thermo Fisher Scientific
Brussels · RemoteSenior (5–10 years)Full-timePosted 5 days ago
About the job
What you'll do
You will lead statistical tasks throughout the clinical trial process, including study design, protocol writing, and final analysis. Additionally, you will collaborate with scientific experts to advance research and ensure high-quality reporting for clinical development programs.
What they're looking for
Candidates must hold an advanced degree with at least 6 years of experience or a bachelor's degree with 8 years of experience in biostatistics. Proficiency in SAS programming, knowledge of ICH-GCP guidelines, and experience with CDISC standards are required.
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