Senior Clinical Research Associate

📋 Description Oversee and monitor clinical trial sites ensuring quality and patient safety. Serve as sponsor point of contact for investigative sites. Train and engage site staff and investigators on trial goals and protocols. Conduct site evaluations, monitoring, and closures per GCP/ICH and AbbVie SOPs. Collaborate with Central Monitoring to detect study risks early. Support compliant trial execution and patient recruitment plans. 🎯 Requirements Health-related tertiary qualification preferred. 3+ years clinically related experience, incl. site monitoring. Knowledge of ICH/GCP, regulatory requirements, and risk-based monitoring. Strong communication and cross-functional collaboration skills. Ability to plan, organize, and manage multiple projects. Proficiency with site engagement tools and data reporting. 🎁 Benefits Equitable, inclusive workplace with flexible, global collaboration. Code of Conduct and business integrity programs. Global opportunities within AbbVie’s R&D network.