• Design, implement, interpret, report and publish the results of retrospective and prospective observational research studies for life sciences customers • Support the development of N-Power Medicine’s data platform and assets, including specification of data models and clinical nomenclature/coding requirements to efficiently harmonize real-world data with clinical trials data standards, such as Clinical Data -Interchange Standards Consortium (CDISC) • Contribute to developing N-Power Medicine’s real-world evidence generation platform, in alignment with the company’s by-protocol, prospective real-time data • Collaborate with internal partners (Clinical Science, Commercial, and Network Partners) to develop the company's strategic partnerships with life sciences • Collaborate with internal partners (Clinical Science, Commercial, and Network Partners) to develop the data requirements to support N-Power Medicine’s next-generation External Controls methodology and product offerings • Help translate the perspectives and requirements of FDA and regulatory agencies around external controls to inform N-Power Medicine's data capture/collection and platform requirements • Ask the right scientific questions, ideate and make recommendations on fit-for-purpose data and analytics solutions • Stay current with novel data analysis methods for observational data, in particular Causal Inference and its applications to clinical trials • Perform additional duties and responsibilities as required