Join Parexel FSP as a Clinical Study Administrator in a hybrid role based in Mississauga, Ontario. Support clinical research by managing documents and coordinating studies from start to finish.

This position involves crucial tasks including interfacing with service providers, ensuring regulatory compliance, and maintaining the eTMF. As the primary administrative contact, your skills in organization and communication will facilitate smooth study operations. The hybrid model allows for three days on-site, fostering close teamwork and support.

Key Responsibilities:
• Coordinate administrative tasks for clinical studies
• Ensure timely submissions to EC/IRB and Regulatory Authorities
• Maintain accurate records in tracking tools like CTMS




• Prepare materials for internal and external meetings
• Manage study materials and equipment logistics

Requirements:
• Secondary school qualifications in a relevant field
• Administrative experience in the medical/life sciences
• Proven organizational and computer skills
• Knowledge of English language and writing
• Ability to work in a team-oriented workplace

Utilize your organizational expertise and communication skills to impact clinical research at Parexel FSP in Mississauga.
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📌 Hybrid Clinical Study Administrator Role (Ontario)
🏢 Parexel
📍 Ontario