Position Overview
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 based in Tokyo or Osaka
You will:
Maintains study-specific and corporate startup tracking systemsFacilitates site budgets and contract negotiationsSupports site regulatory document collectionUnder 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 phaseDevelops site specific startup timelines and enrollment projections and is responsible for meeting the site activation milestonesMay review study specific translationsSupervises Trial Master File (TMF) maintenance throughou...