Become a Senior Clinical Associate at IQVIA in Montréal, contributing to the oversight of clinical trials and ensuring compliance with regulations. Bilingualism in French and English is essential.The ideal candidate has a solid background in site management and at least three years of monitoring experience. Your responsibilities will include conducting comprehensive visits, guiding protocol training at sites, and actively managing recruitment and quality assessment efforts. This role plays a critical part in the success of our clinical studies.Key Responsibilities:Lead site monitoring visits to ensure complianceOptimize subject recruitment and management plansMaintain site communication and training documentationAssess site practices for regulatory quality adherenceManage timelines and financial aspects of site agreementsRequirements:Bachelor's degree in a relevant scientific fieldThree years' experience in clinical site monitoringComprehensive understanding of GCP and ICH practicesProficient in Microsoft Office SuiteExcellent written and verbal communication in English and FrenchUtilize your clinical expertise to make a difference with IQVIA in Montréal.#J-18808-Ljbffr

📌 Senior Clinical Associate At Iqvia Montréal (Montreal)
🏢 IQVIA
📍 Montreal