Clinical Research Associate

Experienced CRA with a passion for oncology research sought to join a highly skilled team at TRIO, a global clinical research organization dedicated to advancing translational cancer research.

Requirements

• Conducting site visits
• Confirming adherence to all FDA, ICH-GCP and local regulations
• Ensuring the completion and collection of regulatory documents
• Performing data verification of source documents
• Ensuring implementation and compliance with FDA, ICH-GCP guidelines

Benefits

• Competitive salary
• Paid annual leave
• Health insurance plan
• Flexible working hours
• Luggage allowance
• Mobile phone allowance