Recruitment

• Assist in monitoring clinical trial sites
• Ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) guidelines
• Support site management activities, including documentation preparation, data entry, and tracking site performance metrics
• Collaborate with cross-functional teams to facilitate communication and address site-related issues
• Maintain accurate records of site activities
• Contribute to the preparation of monitoring reports
• Participate in training and development initiatives to enhance knowledge and skills in clinical trial management

Explore Clinical Study Team Assistant – Patient Recruitment at ICON plc. Review requirements and application details.

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