Contract Biostatistician – Remote (Europe)Remote/Hybrid – Italy or Belgium (Flexible Location)6–12 Month Contract | Competitive Day RateA leading global biopharmaceutical organisation is seeking an experienced Contract Biostatistician to support clinical development programs across multiple therapeutic areas.This role offers the chance to play a key part in all phases of clinical research, working cross-functionally with biometrics, clinical operations, medical affairs, regulatory, and external vendors.Key Responsibilities:Act as project-level statistician for clinical trials from Phase I–IVLead or support statistical planning, analysis, and interpretation for studiesCreate and review statistical analysis plans (SAPs), mock shells, and randomisation schemesPerform or oversee analysis, validation, and statistical reporting for clinical dataCollaborate with internal departments (data management, programming, clinical ops) and external vendorsContribute to regulatory submissions (e.g., FDA, EMA) and support response to statistical queriesProvide input for publications, posters, and conference presentationsRequirements:MSc or PhD in Biostatistics/Statistics or related field5+ years of relevant experience in clinical trials (pharma, biotech, or CRO environment)Strong understanding of clinical trial design, statistical methodology, and regulatory frameworksProficient in SAS; knowledge of R/S-Plus and CDISC (SDTM, ADaM) standards desirableExcellent communication, documentation, and stakeholder engagement skillsPrevious experience with HTA, PK/PD data, or regulatory submissions (BLA/NDA/MAA) is a plusFluent in EnglishWhy apply?Join a collaborative global biometrics teamFlexible working model – remote or hybridEngage in diverse and meaningful projectsOpportunity to work on submission-ready studiesInterested? Apply now to explore this exciting opportunity, or get in touch directly to learn more.