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 workplace.

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
- Strong 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.

📌 Senior Clinical Research Associate Role (Toronto)
🏢 PSI CRO
📍 Toronto