Clinical Trials Specialist

3 days ago


Toronto, Ontario, Canada i-Pharm Consulting Full time

As a Clinical Research Associate at i-Pharm Consulting, you will oversee and manage the progress of clinical trials at investigational sites. This includes ensuring adherence to study protocols, ICH-GCP, and local regulatory requirements.

You will conduct site initiation, monitoring, and close-out visits, providing continuous support to ensure optimal site performance.



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