Apply advanced techniques in measurement techniques in support of Advanced Research and Development products Support stakeholders across R&D, Clinical Affairs, and Regulatory Affairs with insights into clinical trial data analysis for submission to regulatory authorities Work with the biostatistics and data management team to clean and interpret raw data into analysis-ready data sets for submission. Management may, at its discretion, assign or reassign duties and responsibilities to this job at any time. Experience working with human clinical trial data and clinical protocols Experience with statistical languages and packages. Experience with visualization software and techniques. Experience working with JMP, MATLAB, Python, or advanced analysis software Experience performing or evaluating analyses for regulated medical devices. Experience with statistical inference, data mining, pattern recognition or machine learning. Experience with advanced analytic and algorithm techniques for medical device performance characterization from clinical trial data including. Ability to write high quality technical articles for publication in industry and scientific journals. Experience working cross functionally with teams deployed across the US and internationally. Experience in continuous glucose monitoring and related data. Typically requires a Bachelor's degree in a technical discipline, and a minimum of 8-12 years related experience or Master's degree and 5-7 years equivalent industry experience or a PhD and 2-4 years of experience.
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