Posted: 12 November 2026 - Cambridge, United Kingdom
The Senior Clinical Research Associate (Sr. CRA) will oversee the delivery of clinical studies at allocated sites, ensuring compliance with ICH-GCP, local regulations, and study-specific commitments. Responsibilities include site selection, initiation, monitoring, and closure; training site staff; managing enrollment; and preparing monitoring reports. Requires a minimum of 4 years of CRA experience, a Bachelor's degree in a life science discipline, and up to 70% travel. The role supports clinical trials, including rare medical conditions, and collaborates with internal stakeholders and regulatory bodies.