Job Description
This position is a key leadership role within the Quantitative Sciences team, responsible for ensuring rigorous and fit-for-purpose study designs and analyses are performed to meet NPM’s vision and product claims. This role collaborates with a multidisciplinary team to fundamentally change oncology clinical development. Responsibilities include working closely with QS experts, Clinical Science, Product, and other cross functional partners to conduct next generation external control arms (ECAs) that integrate retrospective and prospective real-world data with single arm and randomized clinical trials.
The role develops statistical methodologies that mitigate, observed and unobserved confounding, selection, and measurement bias in external and hybrid controlled studies. Actively supports health system and life science partners, as well as our product portfolio, and develops N-Power Medicine’s real-world evidence generation platform. Leads research study design and end-to-end delivery, including study scoping and the development of study protocols and statistical analysis plans.
About N-Power Medicine
N-Power Medicine aims to establish a new paradigm in drug development by reinventing the ‘how’ and transforming clinical trials.