Enhance your career as a Clinical Trial Coordinator at Parexel in Canada. This role focuses on managing clinical trials and ensuring compliance within regulatory frameworks while working closely with research teams. Parexel seeks motivated Clinical Trial Coordinators to support clinical research managers in various tasks, from trial administration to regulatory submissions. You'll manage essential documents, budget tracking, and study logistics, all while fostering relationships with investigators and sites. A bilingual ability in French and English, along with 1-2 years of relevant experience, is essential for this role.
Key Responsibilities
• Track essential study documents and reports
• Prepare and manage clinical trial documentation
• Support regulatory submissions and protocols
• Develop, track, and report site budgets
• Organize and support investigator meetings
Requirements:
• 1-2 years in clinical research or healthcare
• Bilingual in French and English
• Solid MS Excel and IT skills
• Knowledge of Good Clinical Practices
• Ability to work independently and in teams Play a crucial role in improving patient outcomes through effective trial coordination at Parexel.