Clinical Research Associate

About this role

Responsibilities

• Perform site monitoring visits (selection, initiation, monitoring, and close-out) in accordance with contracted scope of work and regulatory requirements
• Work with sites to adapt, drive, and track subject recruitment plans to enhance predictability
• Administer protocol and study training to assigned sites and establish regular communication to manage project expectations and issues
• Evaluate the quality and integrity of study site practices related to protocol conduct and regulatory adherence
• Manage the progress of assigned studies by tracking regulatory submissions, recruitment, CRF completion, data queries, and submission