
This full-time Senior Clinical Research Associate role is based in the Midwest and Central US, focusing on managing and monitoring clinical trial sites to ensure patient safety and regulatory compliance. The position involves overseeing site operations from activation through close-out, serving as the primary liaison for investigators, and conducting both onsite and remote monitoring to verify data integrity and protocol adherence. Key responsibilities include resolving site-specific issues, supporting patient recruitment, and ensuring adherence to Good Clinical Practices. The role appeals to experienced professionals seeking to work within a dynamic team that values scientific leadership and offers significant opportunities for professional growth in therapeutic areas like oncology. The position requires extensive travel, estimated at 60 to 80 percent, and supports a hybrid work arrangement with remote flexibility.








