Principal Statistician - Early Phase

📋 Description Senior statistical expert supporting clinical studies across all phases of development, from Provide statistical leadership on studies, including design, analysis, randomization, and Develop and oversee Statistical Analysis Plans (SAPs) with specifications, tables, listings, and Support creation/review of analysis datasets, programming specs, and trial documentation. Collaborate with clinical, data management, programming, regulatory, and project management teams Conduct QC reviews of statistical deliverables for accuracy and standards compliance. 🎯 Requirements Graduate degree in Biostatistics, Statistics, Mathematics, or related quantitative field. Extensive experience in clinical trials/biostatistics with ability to lead complex projects. Strong understanding of statistical methods, trial design, analysis techniques, and ICH guidelines. Experience across complete statistical lifecycle: protocol, SAP, analysis, CSR. Proficiency in R programming for clinical research. Regulatory submission experience desirable. 🎁 Benefits Fully remote opportunity from Europe with flexible work arrangements. Opportunity to contribute to meaningful clinical research programs supporting new therapies. Collaboration with international scientific and healthcare teams. Career development through training, mentorship, and exposure to diverse therapeutic areas. Access to a global environment focused on innovation and knowledge sharing. Experience across complex clinical studies and stages of drug development.