About the role
Iterative Health is a healthcare technology and services company powering the acceleration of clinical research to transform patient outcomes. We built a leading performance-driven network of 100+ sites across the US, Europe, India, and Australia, conducting research directly in the communities where care is delivered across gastrointestinal, hepatology, obesity, and cardiology. By combining deep clinical trial expertise with cutting-edge AI, we connect sponsors' scientific ambitions with high-performing research teams that expedite and expand access to novel therapeutics for patients in need. Today, Iterative Health is headquartered in Cambridge, Massachusetts, and New York City with 250+ employees world-wide. As the Project Manager, Clinical Research – New Site Build at Iterative Health for the Cardiology service line, you will lead the end-to-end execution of opening new Cardiology research sites from the ground up. Reporting to the VP, Growth, you will serve as the central project leader responsible for coordinating every aspect of a new site's development—from site selection and facility readiness through regulatory activation, staffing, technology implementation, and study launch. Working cross functionally you'll ensure each site is delivered on time, on budget, and fully prepared to enroll patients. This role is ideal for an experienced project manager who enjoys building new programs, thrives in highly cross-functional environments, and is passionate about expanding patient access to innovative cardiovascular clinical trials. Where You'll Drive Impact Lead the end-to-end project management of de novo Cardiology clinical research site development, from approval through operational launch. Develop and manage comprehensive project plans, timelines, milestones, budgets, and risk registers for each new site. Coordinate cross-functional workstreams across Clinical Operations, Regulatory, Legal, Finance, Real Estate, Facilities, IT, HR, Procurement, and Business Development. Partner with Real Estate and Facilities teams to ensure new sites are designed, built, and equipped to support high-quality clinical research operations. Oversee site activation activities including licensing, regulatory readiness, technology implementation, equipment procurement, SOP deployment, and operational workflows. Coordinate recruiting timelines and onboarding activities with Human Resources to ensure appropriate staffing prior to site launch. Partner with Clinical Operations leadership to establish study startup readiness, investigator onboarding, and research staff training. Identify project risks, dependencies, and operational challenges while proactively developing mitigation plans to maintain timelines. Facilitate regular cross-functional project meetings and provide executive-level status updates to leadership. Develop standardized playbooks, templates, and project management tools to support scalable expansion across future de novo sites. Monitor project budgets, resource allocation, and vendor performance throughout the site development lifecycle. Support continuous process improvement initiatives to enhance speed, consistency, and quality of future site launches. Perform other duties as assigned. What You Bring to
