IQVIA is a global leader in advanced analytics, technology solutions, and clinical research services for the life sciences, enhancing healthcare outcomes through intelligent data connections.
Durham, North Carolina
IQVIA (NYSE:IQV) is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. IQVIA’s portfolio of solutions are powered by IQVIA Connected Intelligence™ to deliver actionable insights and services built on high-quality health data, Healthcare-grade AI™, advanced analytics, the latest technologies and extensive domain expertise. With approximately 88,000 employees in over 100 countries, including experts in healthcare, life sciences, data science, technology and operational excellence, IQVIA is dedicated to accelerating the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. IQVIA is a global leader in protecting individual patient privacy. The company uses a wide variety of privacy-enhancing technologies and safeguards to protect individual privacy while generating and analyzing information on a scale that helps healthcare stakeholders identify disease patterns and correlate with the precise treatment path and therapy needed for better outcomes. IQVIA’s insights and execution capabilities help biotech, medical device and pharmaceutical companies, medical researchers, government agencies, payers and other healthcare stakeholders tap into a deeper understanding of diseases, human behaviors and scientific progress, in an effort to advance healthcare. To learn more, visit www.iqvia.com.
Sur place · Ottawa
The Local Trial Manager oversees clinical trial activities at the country level from start-up to closeout, ensuring high-quality data and regulatory compliance. They collaborate with internal and external stakeholders to manage study budgets, timelines, and site performance.
Sur place · Kirkland
The Senior Clinical Research Associate performs site monitoring visits, including selection, initiation, and close-out, to ensure compliance with GCP and ICH guidelines. They also manage site recruitment plans, oversee regulatory submissions, and maintain essential study documentation.