Lead statistical activities for clinical trials: design, analysis, reporting.
Collaborate with cross-functional teams to ensure regulatory-compliant deliverables.
Support SAPs and CDISC SDTM/ADaM standards compliance.
Contribute to interim analyses and final study reports.

🎯 Requirements

Master’s degree in Statistics, Biostatistics, or related field
0–3 years of relevant experience in clinical research or pharmaceutical industry
Basic knowledge of statistical methods used in clinical trials
Familiarity with regulatory requirements (ICH-GCP)

🎁 Benefits

Global CRO with 28+ years of experience
4,000+ professionals in 20+ countries
Equal opportunity employer focused on diversity and inclusion

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