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 Requirements:
- 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 Make an impact in clinical research operations at ICON plc.

📌 Clinical Trial Coordinator at ICON plc (Montreal)
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📍 Montreal