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 robust background in clinical monitoring, particularly in Oncology and cutting-edge 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
Strong background in Oncology and creative 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.

📌 Lead Clinical Research Associate At Psi Toronto (Canada)
🏢 PSI CRO
📍 Canada