As a Sr. Clinical Research Associate, you will play a key role in coordinating and supervising clinical trials across national and international sites. Your responsibilities include overseeing site activities through a combination of on-site visits and remote monitoring, managing regulatory submissions and supporting trial start-up processes, and collaborating with local CRAs, investigators, and sponsors across multiple countries. You will also contribute to CRF design, data review, and cleaning activities, participate in sponsor and investigator meetings as well as committee support such as CEC and DSMB, and engage with internal teams—including the Core Lab—to ensure alignment across study operations.