Join PSI as a Senior Clinical Research Associate to lead a dynamic research team in optimizing clinical trial management. Focus on compliance and ensure timelines are met.

In this pivotal role at PSI, a leader in contract research, you will leverage your site monitoring experience in a collaborative environment. Your responsibilities will include coordinating the monitoring process, conducting training sessions, and managing data integrity at a regional level. Engage directly with site teams to promote best practices and ensure adherence to various therapeutic protocols.

Key Responsibilities:
• Conduct site audits and manage site-specific training
• Monitor enrollment metrics and implement improvements
• Oversee project team communications and updates




• Lead project meetings focused on compliance and timeline objectives
• Manage CAPA development and implementation processes

Requirements:
• At least 4 years’ experience in clinical monitoring
• Robust familiarity with Oncology research and regulations
• Proven track record in managing clinical teams
• Proficient in MS Office and data management systems
• Willingness to travel frequently for project needs

Shape the future of clinical trials with your expertise and leadership at PSI.
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📌 Senior Clinical Research Associate Role (Ontario)
🏢 PSI CRO
📍 Ontario