(Summary generated by AI based on the full job description)
The project focuses on statistical validation of Digital Health Technologies with emphasis on compliance with FDA and EMA. Required skills include Python (or R) and software development best practices such as Git and unit testing. Responsibilities cover authoring Statistical Analysis Plans, implementing regulatory-grade analytical programming, mapping data into CDISC structures, performing validation analyses (e.g. Bland‑Altman, mixed‑effects models) and compiling regulatory submission documentation. Master's or PhD and at least 6 years of experience in pharmaceutical/medical/CRO sectors are required.




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