Clinical Research Associate
AbbVieRemotely
crmgcpsite monitoringrisk based monitoringichich guidelines
Job Description
📋 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
