Join ICON plc as a Clinical Trial Coordinator, a role crafted for those passionate about clinical research and trial management. This position focuses on the essential tracking and reporting of clinical documentation, alongside effective supply chain management.As a key member of the ICON team, you will support various aspects of clinical trial administration, ensuring that all documentation is properly managed and site evaluations are conducted efficiently. Your responsibilities will also include budget development, regulatory submission preparation, and effective communication with investigators to ensure smooth operations.Key Responsibilities:Track and report essential documents,



including safety reportsManage clinical supply logistics and document workflowsPrepare IRB/ERC submission packages accuratelyDevelop and negotiate site budgets and contractsOrganize and support investigator meetingsRequirements:B.A./B.S. in Life Sciences preferred1-2 years in a relevant clinical research positionAt least 2 years in budget management and negotiationsFully bilingual in French and EnglishProficient IT skills; especially in MS Excel and related softwareEnhance your career and make a difference in clinical research through this role at ICON, where your contributions support cutting-edge healthcare development.

📌 Icon Clinical Trial Coordination Role (Ottawa)
🏢 ICON Strategic Solutions
📍 Ottawa