Clinical Research Associate: Site Monitoring & Impact (Kirkland)

Clinical Research Associate: Site Monitoring & Impact (Kirkland)

18 Oct
|
IQVIA
|
Kirkland

18 Oct

IQVIA

Kirkland

IQVIA is seeking a Site Monitoring qualified to ensure study sites conduct and report data per protocol and sponsor requirements. You will monitor visits, support recruitment plans, and manage regulatory submissions while maintaining TMF/ISF documentation.Communicate with sites and study teams to address issues and keep projects on track. The role requires a science/healthcare degree or equivalent experience, with GCP/ICH knowledge, strong communication, and proficiency in MS Office and

📌 Clinical Research Associate: Site Monitoring & Impact (Kirkland)
🏢 IQVIA
📍 Kirkland

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