Senior Clinical Research Associate

📋 Description Oversee and monitor clinical trial sites to ensure quality, compliance, and patient safety. Act as sponsor point of contact for investigative sites and connect stakeholders. Conduct site evaluation, training, monitoring, and site closure with GCP/ICH adherence. Guide site staff and investigators on protocol and patient treatment principles. Monitor risk signals and collaborate with Central Monitoring to detect study issues. Ensure data quality, timely safety reporting, and regulatory readiness. 🎯 Requirements Teritary qualification in health-related disciplines preferred. Minimum 3 years clinically related experience; 2 years in independent monitoring. Strong knowledge of ICH/GCP, regulatory requirements, and safety reporting. Excellent communication and cross-functional collaboration skills. Strong planning, organization, and site relationship skills. Ability to use technology/tools to support site-focused performance. 🎁 Benefits Competitive compensation and benefits package. Opportunity to work in a global, matrixed environment. Flexible, inclusive work culture with a focus on patient impact.