
This full-time Senior Clinical Research Associate role at Mobius serves as a primary site manager for a diverse portfolio of clinical trials across the USA, Australia, and New Zealand. The position focuses on overseeing the entire trial lifecycle, from study start-up and monitoring to data management and close-out, while ensuring strict adherence to FDA regulations and GCP standards. Key responsibilities include building strong relationships with investigators, troubleshooting compliance issues, mentoring colleagues, and managing project reporting to sponsors. The role appeals to experienced professionals seeking a collaborative environment where they can make a significant impact on bringing new therapies to patients. It offers remote flexibility for candidates in the Midwest, West, and Northeast, with travel required approximately one to two times per week to support US-based projects.
















