
This full-time Senior Clinical Research Associate role focuses on oncology clinical trials within a Fast-paced FSP team based in Northern California. The position involves managing all aspects of site monitoring, including pre-study visits, routine oversight, and close-out procedures to ensure protocol adherence and patient safety. Key responsibilities include verifying informed consent, reviewing data integrity on Case Report Forms, managing Serious Adverse Event reporting, and coordinating with vendors and study staff. The role appeals to candidates seeking a dynamic environment where adaptability and teamwork are essential for success. While the position is designated as remote, it requires significant travel, estimated at 40-50% of the time, to visit clinical sites across the region.
















