Seeking a 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.
* Act as project-level statistician for clinical trials from Phase I–IV
* Lead or support statistical planning, analysis, and interpretation for studies
* Create and review statistical analysis plans (SAPs), mock shells, and randomisation schemes
* Perform or oversee analysis, validation, and statistical reporting for clinical data
* Collaborate with internal departments (data management, programming, clinical ops) and external vendors
A strong understanding of clinical trial design, statistical methodology, and regulatory frameworks is required. Proficiency in SAS and experience with HTA, PK / PD data, or regulatory submissions (BLA / NDA / MAA) are also beneficial. The ideal candidate will be fluent in English and have a flexible working model – remote or hybrid.
Requirements
Key Skills : Strong understanding of clinical trial design, statistical methodology, and regulatory frameworks, proficiency in SAS, experience with HTA, PK / PD data, or regulatory submissions (BLA / NDA / MAA)
Qualifications : MSc or PhD in Biostatistics / Statistics or related field, ~5+ years of relevant experience in clinical trials (pharma, biotech, or CRO environment)
Working Conditions : Flexible working model – remote or hybrid, engage in diverse and meaningful projects
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