Clinical Research Associate 2

📋 Description

• Monitors activities conducted by clinical investigative sites to ensure successful execution of the
• Conducts site qualification, initiation, interim monitoring and study closeout visits for Phase 1-4
• Overviews site personnel activities, motivates teams, maintains regulatory inspection readiness.
• Ensures data quality and timely reporting of safety events by site personnel.
• Trains site personnel on protocol and regulatory requirements with project teams.
• Manages investigator payments, negotiates site/hospital agreements, and completes expense reports.

🎯 Requirements

• Appropriate tertiary qualification in health-related field preferred.
• Minimum 2 years clinically related experience, at least 1 year independent monitoring.
• Knowledge of therapeutic indications related to clinical trials.
• Strong planning, organizational, analytical and communication skills.
• Understanding of regulatory requirements, ICH/GCP and applicable regulations.
• Ethical standards and integrity in business practices.

🎁 Benefits

• Company information and resources available on AbbVie’s global platforms.
• Equal opportunity employer; accommodations available where applicable.