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 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 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.

📌 Lead Clinical Research Associate at PSI (Toronto)
🏢 PSI CRO
📍 Toronto