Senior Clinical Research Associate

📋 Description Oversee and monitor clinical trial sites to ensure quality, compliance, and patient safety. Collaborate with Sponsors, site staff, and investigators to advance trial execution. Train and motivate site staff on trial goals, protocols, and patient treatment principles. Conduct site evaluations, monitoring, and closure activities per SOPs and GCP/ICH. Report adverse events within 24 hours; participate in risk assessment and issue mitigation. Maintain data quality and ensure timely reporting of safety and study data. 🎯 Requirements Tertiary qualification in health-related field preferred. Minimum 3 years clinically related experience; experience in monitoring trials is preferred. Strong knowledge of ICH/GCP, regulatory requirements, and site engagement strategies. Excellent communication, collaboration, planning, and organizational skills. Ability to leverage technology to support site-centric trial delivery. Ability to work in a fast-paced, global environment with multiple projects. 🎁 Benefits Equal opportunity employer and inclusive workplace. Flexible collaboration in an international, matrixed team.