Senior Clinical Research Associate

📋 Description Serve as primary Sponsor contact for investigative sites Train and motivate site staff and PI on trial goals Conduct site evaluation, training, monitoring, and closure Develop site engagement strategy and track progress Link protocol and science to day-to-day trial activities Support recruitment and protocol compliance 🎯 Requirements Health discipline degree (preferred) 3+ years in clinical research monitoring Familiar with risk-based monitoring (RBM) Strong knowledge of ICH/GCP and local regulations Excellent communication and cross-functional collaboration Ability to plan, organize, and manage multiple projects 🎁 Benefits Flexible work arrangements in a matrixed global environment Dedicated learning, development and leadership opportunities Commitment to diversity and inclusion Code of conduct and integrity emphasis