Senior Clinical Research Associate

📋 Description Oversee and monitor clinical trial sites to ensure quality, compliance, and patient safety. Serve as primary Sponsor point of contact for investigative sites and connect stakeholders. Train and align site staff and investigators on trial goals, protocol, and patient treatment Conduct site evaluations, training, and on-site/off-site monitoring per GCP/ICH and AbbVie SOPs. Engage in risk assessment, site management, and regulatory/quality assurance activities to drive 🎯 Requirements Tertiary qualification in health-related disciplines (preferred). Minimum 3 years clinically related experience; 2+ years in independent clinical monitoring. Familiar with risk-based monitoring, onsite/offsite monitoring, and early phase studies desirable. Strong knowledge of regulatory ICH/GCP guidelines and local requirements. Excellent communication and cross-functional collaboration skills, with strong planning and 🎁 Benefits Global, inclusive workplace with flexible work practices. Opportunities to work with a world-class clinical development team. Commitment to integrity, ethics, and employee development.