Job Description
Take your career to the next level and lead challenging study activation process on a country/regional level. You will support clinical research teams and ensure PSI projects start smoothly and on time.
Office Base: Shanghai
You will:
Maintains study-specific and corporate startup tracking systems.Facilitates site budgets and contract negotiations.Supports site regulatory document collection.Under supervision, may prepare initial submission dossiers to competent authorities, ethics committees, and/or site submission dossiers (as applicable).Communicates with the project team and investigational sites throughout the study startup phase.Develops site specific startup timelines and enrollment projections and is responsible for meeting the site activation milestones.May review study specific translations.Supervises Trial Master File (TMF) maintenance throughout ...