Senior Clinical Research Associate (Home Based) - IQVIA Biotech - Belgium

Senior Clinical Research Associate at IQVIA responsible for monitoring clinical trial sites and managing study data collection across biotech projects in Belgium. Role involves site visits, regulatory compliance oversight, recruitment tracking, and documentation management from a home-based location.

Responsibilities

• Conduct site monitoring visits including initiation, ongoing monitoring, and close-out activities
• Work with sites on subject recruitment planning and tracking to meet enrollment targets
• Provide protocol training to sites and maintain regular communication on project expectations
• Evaluate site compliance with protocol requirements and regulatory standards
• Track study progress including CRF completion, data queries, and regulatory submissions

Requirements

• Bachelor's degree in scientific or healthcare discipline
• Minimum 1 year of on-site clinical monitoring experience
• Knowledge of GCP and ICH regulatory guidelines
• Proficiency in Microsoft Office (Word, Excel, PowerPoint)
• Strong written and verbal English communication skills
• Organizational and problem-solving capabilities