The Vice President of Vaccine Clinical Research & Development will oversee and ensure that vaccine clinical research and development programs are planned and implemented to meet company objectives. Responsibilities include leading global clinical research programs, providing high-level oversight, identifying program issues, collaborating with clinical leads, and assuring program quality through oversight and monitoring.

The Site Activation Partner is responsible for leading and supporting operational activities for clinical studies and investigator sites to ensure compliance with study timelines and regulations. This role involves coordinating activities related to IRB/EC packages, essential documents management, and maintaining site compliance throughout the study lifecycle.