Clinical Research Associate – Site Monitoring & Compliance
Merck
96.2K–151K a year
Behavioral Health Market Context
Apply Nowvia Learn4Good
Job Description
Merck is seeking an experienced Clinical Research Associate to manage study sites across assigned protocols, ensuring compliance with ICH-GCP and country regulations. You will be the primary site contact, oversee monitoring activities, and drive site readiness and performance.
The role requires travel and strong collaboration with Investigators, CRAs, and cross-functional teams to maintain data i
The role requires travel and strong collaboration with Investigators, CRAs, and cross-functional teams to maintain data i
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