Clinical Research Associate

📋 Description

• Primary contact for investigative site and driver of trial execution
• Aligns site staff and PI to trial goals and patient treatment principles
• Performs site evaluation, training, monitoring per protocol and GCPs
• Customizes site engagement strategy based on study needs
• Ensures data quality, safety reporting and timely follow-up
• Maintains audit/readiness and oversees investigator payments

🎯 Requirements

• Healthcare/science degree preferred (Medical, Scientific, Nursing)
• Minimum 1 year clinical experience; 6 months in clinical research monitoring
• Familiar with risk-based monitoring; onsite and offsite monitoring
• Knowledgeable in regulatory requirements, ICH/GCP guidelines
• Strong cross-functional collaboration and organizational skills
• Proficiency in Korean (written and spoken) required

🎁 Benefits

• Equal opportunity employer information available
• Opportunity to contribute to AbbVie’s clinical development programs