Elevate your clinical research career with PSI as a Lead Clinical Research Associate. Manage site monitoring and protocols effectively, ensuring data integrity and compliance.
PSI, a renowned Contract Research Organization, seeks a skilled Lead Clinical Research Associate. This role demands a strong background in clinical monitoring, particularly in Oncology and innovative therapies like CAR-T. You will coordinate site feasibility, monitor timelines, implement corrective measures, and ensure adherence to compliance regulations.
Key Responsibilities:
• Coordinate investigator/site feasibility and study startup processes
• Monitor project timelines and patient enrollment for accuracy
• Review monitoring visit reports for compliance and consistency




• Manage query resolution and Central Monitoring observations
• Conduct training for site Investigators and newly promoted Lead CRAs
Requirements:
• Minimum 4 years of site monitoring experience
• Knowledge of US and Canadian regulatory guidelines
• Solid background in Oncology and innovative therapies preferred
• Full working proficiency in English
• Ability to travel up to 65% as needed
Utilize your expertise in clinical research to drive project success and ensure high standards at PSI.
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📌 Lead Clinical Research Associate at PSI (Toronto)
🏢 PSI CRO
📍 Toronto