Excel as a full-time Clinical Research Associate with IQVIA in Kirkland, Quebec, ensuring that clinical trial sites operate efficiently and in compliance with all regulatory standards. Your expertise is crucial for study success.
This role encompasses monitoring visits across study sites, managing relationships with site personnel, and facilitating compliance with Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) standards. You will evaluate site practices, support recruitment plans, and oversee documentation to maintain study integrity.
Key Responsibilities: • Monitor clinical study sites per regulatory and contractual requirements • Track subject recruitment and data submission progress • Deliver training on study protocols at assigned sites • Create and maintain essential project documentation • Liaise with study teams for effective project execution