Integration of patient generated and reported data is at the heart of everything we do at Koneksa. We have built a significant device integration platform that ingests, validates, processes and archives data from multiple devices. This platform needs to handle large volumes of data quickly and in a manner compliant with regulatory authorities. This means thoughtful design and careful engineering.
Your responsibility will be to take over the design and build of the next generation of our device integration platform. This includes high-level design work, engineering improvements to the existing platform and integration of new data streams and features.
You will partner with device vendors and team members to integrate data into Koneksa systems with robust integrity guarantees and full audit trail. You will collaborate with Koneksa data science to produce analytics reports and implement live monitoring of data quality.
The data that flows through these systems will be used in Koneksa scientific reports that will be submitted to academic journals. And, most importantly, this data must ultimately be ready for submission to the FDA in support of new drug applications.
Because this work is so important to our customer and their patients, we require your excellence.
You should be a software engineer with 3+ years of experience, and unseemly levels of talent.
You should understand: