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. #J-18808-Ljbffr

📌 Clinical Trial Start-Up Specialist - Hybrid Role (Winnipeg)
🏢 ManpowerGroup Global
📍 Winnipeg