• Upfront support of Medical Device clinical trials and research, supporting statistical aspects of study design by assisting with sample size calculation via power analysis and study design, and ensuring the protocol and variables collected support the endpoint analysis. • Execute statistical analyses including, but not limited to, established methods such as confidence interval testing, regression models, Bayesian methods, missing data handling, mixed models. • Create reproducible code, summary tables, visualizations, and written statistical outputs that support study reports, technical documents, and defend results to regulatory agencies. • Prepare analysis datasets by performing data cleaning, validation, formatting, and code reviews. • Document statistical approaches and analytical workflows to promote transparency and reproducibility to be documented in the Clinical History File. • Collaborate with cross‑functional partners including Clinical Operations, Quality and Regulatory, engineering, and data management teams to support project execution.