Responsible for project management of clinical research conducted under ethical guidelines or clinical research regulations, including building and overseeing project structures, developing study plans (such as risk management plans), managing timelines and milestones, controlling documentation, budgets, and invoicing, coordinating cross\-functional teams, and serving as the primary contact for vendors and clients.
Requirements
Required qualifications include project management experience in clinical or real\-world evidence research with full understanding of the study process from planning to publication, proven ability in progress tracking and cross\-department coordination, strong proposal and negotiation skills, expertise in a specific disease area, and English proficiency (reading and writing required; speaking preferred).
