Conduct clinical monitoring at PSI across therapeutic indications, applying source verification and query resolution expertise. Travel throughout North America for onsite visits.

As a Clinical Research Associate II, you will support clinical studies while maintaining PSI’s quality standards. The work includes monitoring visits, site management, study startup, and regulatory support. You will communicate with project teams, vendors, and support services throughout study delivery.

Key Responsibilities:
Conduct and report all types of onsite monitoring visits
Perform CRF review and source document verification
Resolve queries and manage site communications
Communicate study progress with internal project teams
Support regulatory documents and feasibility research

Requirements:
Life Sciences degree or equivalent education, training, and experience
Independent North American onsite monitoring experience
Phase II and/or III monitoring visit experience
Full working proficiency in English and French
MS Office proficiency and ability to travel

Apply clinical monitoring, site management, and bilingual communication skills as a Clinical Research Associate II at PSI.
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📌 Clinical Research Associate Ii Monitoring Toronto (Canada)
🏢 PSI CRO
📍 Canada