(Summary generated by AI based on the full job description)
The project focuses on statistical validation of Digital Health Technologies for regulatory compliance. Key technologies include Python (or R), proficiency with Git and unit testing practices, and mapping data into CDISC. Responsibilities include authoring Statistical Analysis Plans, implementing regulatory-grade programming and analyses, performing validation statistics (e.g. Bland-Altman, mixed-effects models), preparing FDA/EMA submission documentation and ensuring compliance with 21 CFR Part 11 and GCP.




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