Elevate your career as a Clinical Trial Coordinator at Parexel FSP, blending your budget negotiation skills with clinical research expertise. This hybrid role requires one day onsite in Kirkland, Quebec.

As a Clinical Trial Coordinator, you will support the Clinical Research Manager throughout the study lifecycle, from initiation to closure. Key tasks include tracking essential documents, managing clinical supplies, and maintaining budget negotiations. Your role will also involve document management and ensuring compliance with regulatory requirements.

Key Responsibilities:
• Track and report essential documents and safety reports
• Update clinical trial databases and trackers
• Prepare and archive clinical documents thoroughly




• Support budget development with finance representatives
• Organize and manage meeting logistics for investigators

Requirements:
• B.A./B.S. in Life Sciences or equivalent healthcare experience
• 1-2 years in Clinical Research or relevant healthcare roles
• Knowledge of Positive Clinical Practice (GCP)
• Proficient in MS Office, especially Excel
• Strong time management and interpersonal skills

Utilize your clinical and financial expertise to drive successful outcomes in clinical trials at Parexel FSP.
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📌 Clinical Trial Coordinator with Budget Focus (Quebec City)
🏢 Parexel
📍 Quebec City