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.