About the job
Iterative Health is at the forefront of transforming clinical research through innovative healthcare technology and services. Our expansive Site Network, comprising over 70 clinical research sites across the U.S. and Europe, is dedicated to accelerating the market entry of cutting-edge gastrointestinal (GI) and hepatology therapies. We are committed to empowering our partner sites with tech-enabled solutions that enhance their success and growth. By integrating profound clinical trial expertise with advanced AI technologies, we enable research teams and study sponsors to broaden and expedite access to novel therapeutics for patients in critical need.
We are pioneering the application of artificial intelligence in gastroenterology to optimize clinical trials. Utilizing sophisticated machine learning and computer vision techniques, we analyze endoscopic videos and other data types, assisting clinicians in accurately diagnosing patients with potential GI issues. Our goal is to establish meaningful endpoints that serve as reliable predictors of therapeutic responses and disease outcomes. This is a thrilling time in the Clinical Research sector as we champion the advancement of research through streamlined processes, aiming to deliver treatment options to patients more swiftly and efficiently.
We are in search of a Clinical Regulatory Specialist to join our dynamic team. This role will report to a Clinical Regulatory Manager or Director and primarily focus on assisting research sites with the execution and compliance of Phase 2-4 pharma-sponsored research studies. As a collaborative individual contributor, you will work closely with internal stakeholders, clinical sites, and study sponsors/CROs, performing results-driven administrative and regulatory functions.