Senior/Principal Statistician Consultant

📋 Description Provide statistical leadership across clinical development programs, from early-phase studies Lead clinical trial design, including endpoint selection, sample size calculations, power analyses Develop and review clinical study protocols, statistical analysis plans (SAPs), and other Oversee statistical analyses and interpretation of clinical trial data to ensure scientific rigor Provide statistical expertise for regulatory submissions and interactions with health authorities Collaborate with Clinical Development, Clinical Operations, Data Management, Regulatory Affairs 🎯 Requirements PhD in Statistics, Biostatistics, or a related quantitative discipline; a Master's degree with Significant experience in biostatistics within the pharmaceutical, biotechnology, or clinical Strong knowledge of clinical trial design, statistical inference, sample size determination, power Proven experience developing and reviewing statistical analysis plans, clinical study protocols Familiarity with regulatory requirements and guidance applicable to clinical development and Experience supporting clinical development programs in oncology, rare diseases, and/or neuroscience. 🎁 Benefits Full-service CRO with over 28 years of proven high-quality delivery Over 4,000 professionals in more than 20 countries across the Americas, Europe, and Asia-Pacific Continuous training and management to develop and maintain highly-qualified personnel Equal opportunity employer with diverse and inclusive culture Below industry average turnover rates