Jiyoon Bae

• Conducted clinical trial in accordance with protocol and recorded and monitored progress.
• Coordinated and scheduled protocol-related visits and required testing to demonstrate vigilance in patient safety, protocol compliance and data quality.
• Collaborated with clinical study site and sponsor to troubleshoot and provide solutions to study-related issues.
• Gathered and organized clinical trial documentation to meet rigorous standards for site approval.
• Conducted initiation, monitoring and closeout visits to verify study procedures, regulatory documents and data completion.
• Maintained site monitoring schedules to facilitate effective communication with members of clinical team.
• Traveled to investigative sites to conduct site qualification, initiation, interim monitoring and close-out visits to maintain and enforce regulatory compliance.

rove long-term health outcomes.

• Promoted a safe and comfortable healing environment by addressing patient concerns promptly and professionally.
• Streamlined communication between patients, families, and healthcare providers to ensure comprehensive understanding of care plans.
• Equipped patients with tools and knowledge needed for speedy and sustained recovery.
• Improved patient satisfaction ratings by delivering compassionate and personalized care.