Explore growth in clinical research as a Clinical Study Administrator with Parexel FSP in Mississauga, Ontario, in a hybrid work setting. You will coordinate and manage clinical studies and ensure compliance with regulatory standards.

In this pivotal role, you will support the administration of studies from their inception through to completion. This includes document preparation, timely submissions, and ensuring training on procedures. Strong focus on detail and excellent organizational skills are key to achieving study objectives effectively.

Key Responsibilities:
• Assist in coordination of clinical study execution
• Handle essential document uploads for eTMF readiness
• Collaborate with investigators and ensure compliance




• Prepare presentation materials for various meetings
• Track and manage study materials and budgets

Requirements:
• High school or equivalent educational qualifications
• Experience in administration within the life sciences field
• Strong organizational skills and computer literacy
• Good English communication skills
• Ability to handle shifting priorities and tasks

Bring your organizational skills and passion for clinical research to Parexel FSP in Mississauga.
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📌 Clinical Research Administration at Parexel (Ontario)
🏢 Parexel
📍 Ontario