A pioneering healthcare company based in the United States seeks a Regulatory Affairs professional to lead the strategy and execution of regulatory submissions, particularly in the domain of early cancer detection. The ideal candidate will have at least 10 years of experience in the regulatory landscape, specifically in the IVD, medical device, or pharmaceutical sectors. Key responsibilities include preparing FDA submissions, collaborating with internal departments, and ensuring compliance with regulatory requirements. This role offers a competitive salary range of $164K-$205K.#J-18808-Ljbffr