Senior Clinical Research Associate

📋 Description Oversee and monitor clinical trial sites to ensure quality, compliance, and patient safety. Act as primary sponsor point of contact for investigative sites, connecting stakeholders. Train and motivate site staff and investigators on trial goals, protocols, and patient treatment Conduct site evaluation, training, monitoring, and site closure with adherence to GCPs and AbbVie Identify and engage investigators/sites to support planned studies with qualified investigators. Ensure data quality and timely reporting, including safety events and regulatory readiness. 🎯 Requirements Appropriate tertiary qualification in health-related disciplines (preferred). Minimum 3 years clinically related experience; 2 years in independent clinical research monitoring. Experience in Early Phase 1 and First-in-Human studies desirable. Strong knowledge of regulatory requirements, ICH/GCP, and applicable policies. Excellent communication and cross-functional collaboration skills. Ability to plan, organize, and manage multiple projects in a dynamic environment. 🎁 Benefits AbbVie equal opportunity workplace with inclusive culture. Global collaboration in a matrix environment; flexible and supportive policies.