Become a Clinical Trial Start-Up Specialist with our client in Mississauga, ON, working in a hybrid mode. Contribute to global trial initiation efforts and streamline site activation processes.

This role in the Clinical Operations department requires a blend of strong communication, organizational skills, and collaboration. As a Clinical Trial Start-Up Specialist, you will lead the country strategy for study start-up, ensuring efficiency with external stakeholders while managing compliance and operational timelines.

Key Responsibilities:
• Lead study start-up strategy for operational efficiency
• Oversee timely site activation and regulatory submissions
• Align local processes with global strategies




• Manage amendments throughout the study lifecycle
• Identify and drive innovation in start-up workflows

Requirements:
• Degree in life sciences or equivalent; master's preferred
• Proven clinical trial start-up experience and regulatory knowledge
• Strong understanding of ICH-GCP and local regulations
• Experience managing vendor and CRO relationships
• Excellent communication and analytical skills

Shape the future of clinical research with expertise in trial start-up and regulatory compliance.
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📌 Clinical Trial Start-Up Specialist - Hybrid Role (Ontario)
🏢 ManpowerGroup Global
📍 Ontario