Clinical Research Associate

📋 Description

• Primary point of contact for investigative sites.
• Aligns and trains site staff and principal investigators on trial goals.
• Conducts site evaluation, training, monitoring, and close-out activities with GCP/ICH compliance.
• Advances site engagement strategy and uses CRM tools to report progress.
• Ensures data submit quality and timely safety reporting by site personnel.
• Maintains audit/inspection readiness and site risk mitigation.

🎯 Requirements

• Healthcare-related tertiary qualification preferred.
• Minimum 1 year clinically related experience; 6 months in clinical research monitoring.
• Familiar with risk-based monitoring, onsite and offsite monitoring.
• Knowledge of ICH/GCP guidelines and local regulatory requirements.
• Strong cross-functional collaboration and project organization skills.
• Ability to mentor others and leverage technology for site-centric support.

🎁 Benefits

• Equal opportunity employer information and disclosures may apply.
• AbbVie information and links provided in company materials.