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Parexel is seeking a Clinical Research Associate to act as the primary site contact and site manager across all phases of a clinical study. You will ensure site readiness and compliance with ICH-GCP, Sponsor SOPs, and local regulations while coordinating monitoring visits and regulatory documentation.
The role requires 2+ years of direct site monitoring experience in bio/pharma/CRO, a science-oriented degree, and the ability to travel extensively (65–75%).
Parexel is seeking a Clinical Research Associate to act as the primary site contact and site manager across all phases of a clinical study. You will ensure site readiness and compliance with ICH-GCP, Sponsor SOPs, and local regulations while coordinating monitoring visits and regulatory documentation.
The role requires 2+ years of direct site monitoring experience in bio/pharma/CRO, a science-oriented degree, and the ability to travel extensively (65–75%).