CRA I

📋 Description Act as primary contact for investigative sites, sharing trial context and coordinating with AbbVie Align and train site staff and principal investigators on trial goals, protocol, and treatment Conduct site evaluations, training, monitoring, and site closures per protocol and regulatory Customize site engagement strategy using tools like CRM to report progress and measure impact. Support recruitment and retention planning based on patient journey and disease area knowledge. Monitor risk with Central Monitoring team to ensure study performance and patient safety. 🎯 Requirements Appropriate tertiary qualification in health-related fields or equivalent experience. Experience in clinical research coordinating or data management preferred. Knowledge of therapeutic areas and ICH/GCP guidelines and policies. Strong collaboration, planning, and organizational skills in dynamic environments. Ability to leverage technology for customer-centric site support and issue resolution. Excellent communication and relationship-building skills to foster trusted partnerships. 🎁 Benefits Equal opportunity employer information may apply. Company information and social links available in the job description.