Advance your career as a Clinical Research Associate for PSI, overseeing clinical trials and ensuring compliance with regulatory standards. Focus on patient enrollment and data integrity.

PSI is looking for a qualified Clinical Research Associate with a strong background in site monitoring and clinical trial management. This role provides chance to work on diverse therapeutic indications while leading site training and monitoring efforts. Your expertise will help guide project timelines and ensure adherence to safety protocols.

Key Responsibilities:
• Monitor project timelines for accurate patient enrollment
• Supervise query resolution and data verification processes
• Conduct required safety information flow reporting




• Ensure timely updates to study tracking systems
• Provide training and mentorship to project team members

Requirements:
• Relevant degree in Life Sciences or equivalent
• Minimum 4 years of clinical monitoring experience
• Knowledge of CAR-T and GI therapies preferred
• Strong communication and problem-solving skills
• Ability to travel extensively based on project demands

Bring your clinical research expertise to PSI and contribute to impactful therapeutic developments.
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📌 Clinical Research Associate with PSI (Ontario)
🏢 PSI CRO
📍 Ontario