Clinical Trial Coordinator at ICON plc

Join ICON plc as a Clinical Trial Coordinator in Montreal, where you will be pivotal in managing clinical trial operations and documentation. Utilize your communication and organizational skills to ensure success. As a Clinical Trial Coordinator, you will handle trial administration, manage essential documents, and collaborate on regulatory submissions. The role requires 1-2 years of clinical research experience and fluency in both French and English. You will also oversee budgeting and coordinate investigator meetings. Key Responsibilities:

• Facilitate site administration and documentation tracking
• Manage updates to clinical trial management systems
• Prepare and archive clinical trial documents effectively
• Collaborate on regulatory submissions and insurance tracking
• Plan and organize meetings for study teams

• Minimum of 1-2 years in Clinical Research or healthcare
• Fluent in French and business proficient in English
• Understanding of global and local clinical research guidelines
• Proficient IT skills, focusing on document management
• Must be legally authorized to work in Canada