Mar 11, 2026
Biogen
About This Role This role is part of the Clinical Trial Accelerator Unit (CTAU) and is responsible for accelerating Study Start Up activities and ensuring all site activations are made on time in global clinical studies. The individual will harmonize processes and provide start-up expertise to assigned studies and programs, ensuring study teams meet or exceed Final Protocol to First Patient In timelines. The role involves direction and execution, quality compliance, risk management, performance monitoring and cross-functional collaboration. What You'll Do Lead and oversee the execution of site activation for global clinical studies Develop and maintain critical path and timelines for site activation Oversee and negotiate timelines for Master Informed Consent Forms (ICFs), including country and site-level ICF creation. Ensure site activation activities are inspection-ready and compliant with ICH-GCP and Biogen SOPs Perform or delegate quality checks on...
Professional Diversity Network
Boston, MA, USA
Full-Time
